Diaminotriazine derivatives as herbicides

ABSTRACT

The present invention relates to diaminotriazine compounds of the formula (I) and to their use as herbicides. The present invention also relates to agrochemical compositions for crop protection and to a method for controlling unwanted vegetation. 
     
       
         
         
             
             
         
       
         
         
           
             wherein 
             q is 0, 1, 2 or 3 
             R a  is selected from the group consisting of C 1 -C 6 -haloalkoxy, C 1 -C 6 -haloalkylthio, (C 1 -C 6 -haloalkyl)sulfinyl, (C 1 -C 6 -haloalkyl)-carbonyl, etc.; 
             R b  is selected from the group consisting of halogen, OH, CN, amino, NO 2 , C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -alkoxy, etc.; 
             R 1  is selected from the group consisting of H, OH, S(O) 2 NH 2 , CN, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, (C 3 -C 6 -cycloalkyl)-C 1 -C 4 -alkyl, etc.; 
             R 2  is selected from the group consisting of H, OH, S(O) 2 NH 2 , CN, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, (C 3 -C 6 -cycloalkyl)-C 1 -C 4 -alkyl, etc.; 
             R 3  is selected from the group consisting of H, halogen, OH, CN, C 1 -C 6 -alkyl, (C 1 -C 6 -alkoxy)-C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl, etc.; 
             R 4  is H, halogen, CN, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -halocycloalkyl, C 1 -C 6 -alkoxy and C 1 -C 6 -haloalkoxy; 
             R 5  is selected from the group consisting of halogen, CN, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 3 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, etc.; or 
             R 4  and R 5  together with the carbon atom to which they are attached form a moiety selected from the group consisting of carbonyl, C 3 -C 6 -cycloalkan-1,1-diyl, ipso-C 3 -C 6 -cycloalkendiyl, three- to six-membered saturated or partially unsaturated ipso-heterocyclodiyl; 
             including their agriculturally acceptable salts.

The present invention relates to diaminotriazine compounds and to theiruse as herbicides. The present invention also relates to agrochemicalcompositions for crop protection and to a method for controllingunwanted vegetation.

U.S. Pat. No. 3,816,419 describes 4-haloalkyl or4-haloalkenyl-2,4-diaminotriazines and their use as herbicides. Similarcompounds are known from U.S. Pat. No. 3,932,167. The amino groups ofthese compounds do not carry an ortho-fluora-phenyl radical.

DE 197 44 711 describes herbicidally active 2,4-diamino-1,3,5-triazinecompounds, which carry a group A-Z in the 6-position, where A isalkylene and Z is a carbocylic or heterocyclic radical.

DE 198 30 902 describes amino-chloro-triazine compounds and their use asherbicides.

EP 0545 149 describes 6-trifluoromethyl-1,3,5-triazine compounds andtheir use as intermediates for crop protecting agents.

DE 195 31 084 describes diamino-1,3,5-triazine derivatives, wherein oneof the amino groups attached to the triazine ring bears a phenyl-alkylradical. The amino groups of theses compounds do not carry anortho-fluoro-phenyl radical.

However, the herbicidal properties of the known triazine type compoundsare not always entirely satisfactory.

Earlier filed PCT/EP2013/072055 describes2-(o-fluorophenyl)amino-6-aminotriazine compounds having herbicideactivity.

Earlier filed EP 13176634.7 describes 2-(hetaryl)amino-6-aminotriazinecompounds having herbicide activity.

It is an object of the present invention to provide compounds havingimproved herbicidal action, in particular good herbicide activity at lowapplication rates. Moreover, the herbicids should be sufficientlycompatible with crop plants for commercial utilization.

These and further objects are achieved by diaminotriazine compounds offormula (I), defined below, and by their agriculturally suitable salts.

Accordingly, the present invention relates to diaminotriazine compoundsof formula (I)

wherein

-   -   q is 0, 1, 2 or 3    -   R^(a) is selected from the group consisting of C₁-C₆-haloalkoxy,        C₁-C₆-haloalkylthio, (C₁-C₆-haloalkyl)sulfinyl,        (C₁-C₆-haloalkyl)-carbonyl, (C₁-C₆-haloalkyl)sulfonyl,        C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy,        C₂-C₆-haloalkynyloxy, (C₁-C₆-haloalkoxy)-C₁-C₆-alkoxy,        (C₁-C₆-alkyl)-carbonyloxy, (C₁-C₆-haloalkyl)-carbonyloxy,        C₃-C₆-cycloalkoxy, C₃-C₆-halocycloalkoxy,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy,        (C₃-C₆-halocycloalkyl)-C₁-C₄-alkoxy,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl,        (C₃-C₆-halocycloalkyl)-C₁-C₄-alkyl,        (C₃-C₆-cycloalkoxy)-C₁-C₄-alkyl,        (C₃-C₆-halocycloalkoxy)-C₁-C₄-alkyl,        (C₃-C₆-cycloalkyl)-carbonyloxy, (C₁-C₆-alkoxy)-C₁-C₆-alkoxy;    -   R^(b) is selected from the group consisting of halogen, OH, CN,        amino, NO₂, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,        C₁-C₆-alkoxy, C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy,        (C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkoxy)-C₁-C₆-alkoxy,        (C₁-C₆-alkoxy)-C₂-C₆-alkenyl, (C₁-C₆-alkoxy)-C₂-C₆-alkynyl,        C₁-C₆-alkylthio, (C₁-C₆-alkyl)sulfinyl, (C₁-C₆-alkyl)sulfonyl,        (C₁-C₆-alkyl)amino, di(C₁-C₆-alkyl)amino,        (C₁-C₆-alkyl)-carbonyl, (C₁-C₆-alkoxy)-carbonyl,        (C₁-C₆-alkyl)-carbonyloxy, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkoxy,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy,        (C₃-C₆-cycloalkoxy)-C₁-C₄-alkyl, (C₃-C₆-cycloalkyl)-carbonyloxy,        where the aliphatic and cycloaliphatic parts of the 24        aforementioned radicals are unsubstituted, partly or completely        halogenated and where the cycloaliphatic parts of the last 6        mentioned radicals may carry 1, 2, 3, 4, 5 or 6 methyl groups,        -   for q=2 or 3 it being possible that R^(b) are identical or            different;    -   R¹ is selected from the group consisting of H, OH, S(O)₂NH₂, CN,        C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₁-C₆-alkoxy,        (C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkyl)carbonyl,        (C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl,        (C₁-C₆-alkyl)sulfonyl, (C₁-C₆-alkylamino)carbonyl,        di(C₁-C₆-alkyl)aminocarbonyl, (C₁-C₆-alkylamino)sulfonyl,        di(C₁-C₆-alkyl)aminosulfonyl and (C₁-C₆-alkoxy)sulfonyl, where        the aliphatic and cycloaliphatic parts of the 15 aforementioned        radicals are unsubstituted, partly or completely halogenated,        -   phenyl, phenyl-C₁-C₆-alkyl, phenylsulfonyl,            phenylaminosulfonyl, phenylcarbonyl and phenoxycarbonyl,        -   wherein phenyl in the last 6 mentioned radicals are            unsubstituted or substituted by 1, 2, 3, 4 or 5 identical or            different substituents selected from the group consisting of            halogen, CN, NO₂, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy            and C₁-C₆-haloalkoxy;    -   R² is selected from the group consisting of H, OH, S(O)₂NH₂, CN,        C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₁-C₆-alkoxy,        (C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkyl)carbonyl,        (C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl,        (C₁-C₆-alkyl)sulfonyl, (C₁-C₆-alkylamino)carbonyl,        di(C₁-C₆-alkyl)aminocarbonyl, (C₁-C₆-alkylamino)sulfonyl,        di(C₁-C₆-alkyl)aminosulfonyl and (C₁-C₆-alkoxy)sulfonyl, where        the aliphatic and cycloaliphatic parts of the 15 aforementioned        radicals are unsubstituted, partly or completely halogenated,        -   phenyl, phenylsulfonyl, phenylaminosulfonyl, phenyl-C₁-C₆            alkyl, phenoxy, phenylcarbonyl and phenoxycarbonyl,        -   wherein phenyl in the last 6 mentioned radicals is            unsubstituted or substituted by 1, 2, 3, 4 or 5 identical or            different substituents selected from the group consisting of            halogen, CN, NO₂, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy            and C₁-C₆-haloalkoxy;    -   R³ is selected from the group consisting of H, halogen, OH, CN,        C₁-C₆-alkyl, (C₁-C₆-alkoxy)-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyloxy,        C₂-C₆-alkynyloxy, C₃-C₆-cycloalkoxy,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy, where the aliphatic and        cycloaliphatic parts of the 9 aforementioned radicals are        unsubstituted, partly or completely halogenated;    -   R⁴ is selected from the group consisting of H, halogen, CN,        C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl,        C₃-C₆-halocycloalkyl, C₁-C₆-alkoxy and C₁-C₆-haloalkoxy;    -   R⁵ is selected from the group consisting of halogen, CN,        C₁-C₆-alkyl, C₂-C₆-alkenyl, C₃-C₆-alkynyl, C₃-C₆-cycloalkyl,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₃-C₆-cycloalkenyl and        C₁-C₆-alkoxy-C₁-C₆-alkyl, where the aliphatic and cycloaliphatic        parts of the 7 aforementioned radicals are unsubstituted, partly        or completely halogenated; or    -   R⁴ and R⁵ together with the carbon atom to which they are        attached may form a moiety selected from the group consisting of        carbonyl, C₃-C₆-cycloalkan-1,1-diyl, ipso-C₃-C₆-cycloalkendiyl,        three- to six-membered saturated or partially unsaturated        ipso-heterocyclodiyl, where the carbocycle and the heterocycle        are unsubstituted, partly or completely halogenated or carry        from 1 to 6 C₁-C₆-alkyl groups, and the moiety >C═CR^(x)R^(y),        where R^(x) and R^(y) are hydrogen, C₁-C₄-alkyl or        C₁-C₄-haloalkyl;    -   including their agriculturally acceptable salts.

The present invention relates also to diaminotriazine compound offormula (I)

wherein

-   -   q is 0, 1, 2 or 3    -   R^(a) is selected from the group consisting of C₁-C₆-haloalkoxy,        C₁-C₆-haloalkylthio, (C₁-C₆-haloalkyl)sulfinyl,        (C₁-C₆-haloalkyl)-carbonyl, (C₁-C₆-haloalkyl)sulfonyl,        C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy,        C₂-C₆-haloalkynyloxy, (C₁-C₆-haloalkoxy)-C₁-C₆-alkoxy,        (C₁-C₆-alkyl)-carbonyloxy, (C₁-C₆-haloalkyl)-carbonyloxy,        C₃-C₆-cycloalkoxy, C₃-C₆-halocycloalkoxy,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy,        (C₃-C₆-halocycloalkyl)-C₁-C₄-alkoxy,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl,        (C₃-C₆-halocycloalkyl)-C₁-C₄-alkyl,        (C₃-C₆-cycloalkoxy)-C₁-C₄-alkyl,        (C₃-C₆-halocycloalkoxy)-C₁-C₄-alkyl,        (C₃-C₆-cycloalkyl)-carbonyloxy, (C₃-C₆-cycloalkyl)-carbonyloxy;    -   R^(b) is selected from the group consisting of halogen, OH, CN,        amino, NO₂, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,        C₁-C₆-alkoxy, C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy,        (C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkoxy)-C₁-C₆-alkoxy,        (C₁-C₆-alkoxy)-C₂-C₆-alkenyl, (C₁-C₆-alkoxy)-C₂-C₆-alkynyl,        C₁-C₆-alkylthio, (C₁-C₆-alkyl)sulfinyl, (C₁-C₆-alkyl)sulfonyl,        (C₁-C₆-alkyl)amino, di(C₁-C₆-alkyl)amino,        (C₁-C₆-alkyl)-carbonyl, (C₁-C₆-alkoxy)-carbonyl,        (C₁-C₆-alkyl)-carbonyloxy, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkoxy,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy,        (C₃-C₆-cycloalkoxy)-C₁-C₄-alkyl, (C₃-C₆-cycloalkyl)-carbonyloxy,        where the aliphatic and cycloaliphatic parts of the 24        aforementioned radicals are unsubstituted, partly or completely        halogenated and where the cycloaliphatic parts of the last 6        mentioned radicals may carry 1, 2, 3, 4, 5 or 6 methyl groups,        -   for q=2 or 3 it being possible that R^(b) are identical or            different;    -   R¹ is selected from the group consisting of H, OH, S(O)₂NH₂, CN,        C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₁-C₆-alkoxy,        (C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkyl)carbonyl,        (C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl,        (C₁-C₆-alkyl)sulfonyl, (C₁-C₆-alkylamino)carbonyl,        di(C₁-C₆-alkyl)aminocarbonyl, (C₁-C₆-alkylamino)sulfonyl,        di(C₁-C₆-alkyl)aminosulfonyl and (C₁-C₆-alkoxy)sulfonyl, where        the aliphatic and cycloaliphatic parts of the 15 aforementioned        radicals are unsubstituted, partly or completely halogenated,        -   phenyl, phenyl-C₁-C₆-alkyl, phenylsulfonyl,            phenylaminosulfonyl, phenylcarbonyl and phenoxycarbonyl,        -   wherein phenyl in the last 6 mentioned radicals are            unsubstituted or substituted by 1, 2, 3, 4 or 5 identical or            different substituents selected from the group consisting of            halogen, CN, NO₂, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy            and C₁-C₆-haloalkoxy;    -   R² is selected from the group consisting of H, OH, S(O)₂NH₂, CN,        C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₁-C₆-alkoxy,        (C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkyl)carbonyl,        (C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl,        (C₁-C₆-alkyl)sulfonyl, (C₁-C₆-alkylamino)carbonyl,        di(C₁-C₆-alkyl)aminocarbonyl, (C₁-C₆-alkylamino)sulfonyl,        di(C₁-C₆-alkyl)aminosulfonyl and (C₁-C₆-alkoxy)sulfonyl, where        the aliphatic and cycloaliphatic parts of the 15 aforementioned        radicals are unsubstituted, partly or completely halogenated,        -   phenyl, phenylsulfonyl, phenylaminosulfonyl, phenyl-C₁-C₆            alkyl, phenoxy, phenylcarbonyl and phenoxycarbonyl,        -   wherein phenyl in the last 6 mentioned radicals is            unsubstituted or substituted by 1, 2, 3, 4 or 5 identical or            different substituents selected from the group consisting of            halogen, CN, NO₂, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy            and C₁-C₆-haloalkoxy;    -   R³ is selected from the group consisting of H, halogen, OH, CN,        C₁-C₆-alkyl, (C₁-C₆-alkoxy)-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyloxy,        C₂-C₆-alkynyloxy, C₃-C₆-cycloalkoxy,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy, where the aliphatic and        cycloaliphatic parts of the 9 aforementioned radicals are        unsubstituted, partly or completely halogenated;    -   R⁴ is selected from the group consisting of H, halogen, CN,        C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl,        C₃-C₆-halocycloalkyl, C₁-C₆-alkoxy and C₁-C₆-haloalkoxy;    -   R⁵ is selected from the group consisting of halogen, CN,        C₁-C₆-alkyl, C₂-C₆-alkenyl, C₃-C₆-alkynyl, C₃-C₆-cycloalkyl,        (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₃-C₆-cycloalkenyl and        C₁-C₆-alkoxy-C₁-C₆-alkyl, where the aliphatic and cycloaliphatic        parts of the 7 aforementioned radicals are unsubstituted, partly        or completely halogenated; or    -   R⁴ and R⁵ together with the carbon atom to which they are        attached may form a moiety selected from the group consisting of        carbonyl, C₃-C₆-cycloalkan-1,1-diyl, ipso-C₃-C₆-cycloalkendiyl,        three- to six-membered saturated or partially unsaturated        ipso-heterocyclodiyl, where the carbocycle and the heterocycle        are unsubstituted, partly or completely halogenated or carry        from 1 to 6 C₁-C₆-alkyl groups, and the moiety >C═CR^(x)R^(y),        where R^(x) and R^(y) are hydrogen, C₁-C₄-alkyl or        C₁-C₄-haloalkyl;    -   including their agriculturally acceptable salts.

The present invention also relates to agrochemical compositionscomprising at least one diaminotriazine compound of formula (I) and atleast one auxiliary customary for formulating crop protection agents.

The present invention also relates to the use of diaminotriazinecompounds of formula (I) as herbicides, i.e. for controlling unwantedand/or harmful vegetation or plants.

The present invention furthermore provides a method for controllingunwanted plants. The method includes allowing a herbicidally effectiveamount of at least one diaminotriazine compound of the formula (I) toact on the unwanted plants or vegetation, their seeds and/or theirhabitat. Application can be done before, during and/or after, preferablyduring and/or after, the emergence of the unwanted plants.

Moreover, the invention relates to processes for preparingdiaminotriazine compound of formula (I) and to intermediates.

Further embodiments of the present invention are evident from theclaims, the description and the examples. It is to be understood thatthe features mentioned above and still to be illustrated below of thesubject matter of the invention can be applied not only in thecombination given in each particular case but also in othercombinations, without leaving the scope of the invention.

As used herein, the terms “controlling” and “combating” are synonyms.

As used herein, the terms “undesirable vegetation”, “unwantedvegetation”, unwanted plants” and “harmful plants” are synonyms.

In the context of substituents, the term “one or more substitutents”means that the number of substituents is e.g. from 1 to 10, inparticular 1, 2, 3, 4, 5, 6, 7 or 8.

If the diaminotriazine compounds of formula (I) as described herein iscapable of forming geometrical isomers, for example E/Z isomers, theinvention relates to both the pure isomers and mixtures thereof.Likeweise, the invention relates to the use of the pure pure isomers andto the use of their mixtures and to compositions containing the pureisomers or mixtures thereof.

If the diaminotriazine compounds of formula (I) as described herein haveone or more centres of chirality, e.g. if the substituents R³, R⁴ and R⁵are different from each other, and, as a consequence, are present asenantiomers or diastereomers, the invention relates to both the pureenantiomers or diastereomers, and mixtures thereof. Likeweise, theinvention relates to the use of the pure enantiomers or diasteremers andto the use of the mixtures thereof and to compositions containing thepure enantiomers or diastereomers or mixtures thereof.

If the diaminotriazine compounds of formula (I) as described herein haveionizable functional groups, they can also be employed in the form oftheir agriculturally acceptable salts. Suitable are, in general, thesalts of those cations and the acid addition salts of those acids whosecations and anions, respectively, have no adverse effect on the activityof the active compounds.

Preferred cations are the ions of the alkali metals, preferably oflithium, sodium and potassium, of the alkaline earth metals, preferablyof calcium and magnesium, and of the transition metals, preferably ofmanganese, copper, zinc and iron, further ammonium and substitutedammonium in which one to four hydrogen atoms are replaced byC₁-C₄-alkyl, hydroxy-C₁-C₄-alkyl, (C₁-C₄-alkoxy)-C₁-C₄-alkyl,hydroxy-(C₁-C₄-alkoxy)-C₁-C₄-alkyl, phenyl or benzyl, preferablyammonium, methylammonium, isopropylammonium, dimethylammonium,diisopropylammonium, trimethylammonium, heptylammonium, dodecylammonium,tetradecylammonium, tetramethylammonium, tetraethylammonium,tetrabutylammonium, 2-hydroxyethyl-ammonium (olamine salt),2-(2-hydroxyeth-1-oxy)eth-1-ylammonium (diglycolamine salt),di(2-hydroxyeth-1-yl)-ammonium (diolamine salt),tris(2-hydroxyethyl)ammonium (trolamine salt),tris(2-hydroxypropyl)ammonium, benzyltrimethylammonium,benzyltriethylammonium, N,N,N-trimethylethanolammonium (choline salt),furthermore phosphonium ions, sulfonium ions, preferablytri(C₁-C₄-alkyl)sulfonium, such as trimethylsulfonium, and sulfoxoniumions, preferably tri(C₁-C₄-alkyl)sulfoxonium, and finally the salts ofpolybasic amines such as N,N-bis-(3-aminopropyl)methylamine anddiethylenetriamine.

Anions of useful acid addition salts are primarily chloride, bromide,fluoride, iodide, hydrogensulfate, methylsulfate, sulfate,dihydrogenphosphate, hydrogenphosphate, nitrate, bicarbonate, carbonate,hexafluorosilicate, hexafluorophosphate, benzoate and also the anions ofC₁-C₄-alkanoic acids, preferably formate, acetate, propionate andbutyrate.

Further embodiments of the present invention are evident from theclaims, the description and the examples. It is to be understood thatthe features mentioned above and still to be illustrated below of thesubject matter of the invention can be applied not only in thecombination given in each particular case but also in othercombinations, without leaving the scope of the invention.

The organic moieties mentioned in the definition of the variables, e.g.R¹, R², R³, R⁴, R⁴, R⁵, R^(a) or R^(b) are—like the termhalogen—collective terms for individual enumerations of the individualgroup members. The term halogen denotes in each case fluorine, chlorine,bromine or iodine. All hydrocarbon chains, i.e. all alkyl, haloalkyl,alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl,(alkyl)amino, di(alkyl)amino, alkoxyalkyl, alkoxyalkoxy, (alky)carbonyl,(alkoxy)carbonyl chains can be straight-chain or branched, the prefixC_(n)-C_(m) denoting in each case the possible number of carbon atoms inthe group. The same applies to composed radicals, such ascycloalkylalkyl and phenylalkyl.

Examples of such meanings are:

C₁-C₄-alkyl and also the C₁-C₄-alkyl moieties of C₁-C₄-alkoxy,C₁-C₄-alkylthio, C₁-C₄-alkylsulfonyl, (C₁-C₄-alkyl)carbonyl,(C₁-C₄-alkyl)carbonyl, (C₁-C₄-alkoxy)carbonyl, (C₁-C₄-alkyl)carbonyloxy,C₁-C₄-alkyoxy-C₁-C₄-alkyl, C₃-C₆-cycloalkyl-C₁-C₄-alkyl,(C₁-C₄-alkylamino)carbonyl, di(C₁-C₄-alkyl)aminocarbonyl,(C₁-C₄-alkylamino)sulfonyl, di(C₁-C₄-alkyl)aminosulfonyl orphenyl-C₁-C₄-alkyl: for example CH₃, C₂H₅, n-propyl, CH(CH₃)₂, n-butyl,CH(CH₃)—C₂H₅, CH₂—CH(CH₃)₂ and C(CH₃)₃;

C₁-C₆-alkyl and also the C₁-C₆-alkyl moieties of C₁-C₆-alkoxy,C₁-C₆-alkylthio, C₁-C₆-alkylsulfonyl, (C₁-C₆-alkyl)carbonyl,(C₁-C₆-alkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl, (C₁-C₆-alkyl)carbonyloxy,C₁-C₆-alkyoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,(C₁-C₆-alkylamino)carbonyl, di(C₁-C₆-alkyl)aminocarbonyl,(C₁-C₆-alkylamino)sulfonyl, di(C₁-C₆-alkyl)aminosulfonyl orphenyl-C₁-C₆-alkyl: C₁-C₄-alkyl as mentioned above, and also, forexample, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl,2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1,1-dimethylpropyl,1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl,4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl,2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl,2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl,1-ethyl-1-methylpropyl or 1-ethyl-2-methylpropyl, preferably methyl,ethyl, n-propyl, 1-methylethyl, n-butyl, 1,1-dimethylethyl, n-pentyl orn-hexyl;

C₂-C₆-alkenyl and also the C₂-C₆-alkenyl moieties of(C₁-C₆-alkoxy)-C₂-C₆-alkenyl: a linear or branched ethylenicallyunsaturated hydrocarbon group having 2 to 6 carbon atoms and aC═C-double bond in any position, such as ethenyl, 1-propenyl,2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl, 3-butenyl,1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl,2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl,1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl,1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl,1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl,1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl,1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl,1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl,1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl,4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl,3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl,2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl,1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl,4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl,1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl,1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl,2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl,2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3-dimethyl-2-butenyl,1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl,2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl,1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl,1-ethyl-2-methyl-1-propenyl and 1-ethyl-2-methyl-2-propenyl;

C₂-C₆-alkynyl and also the C₂-C₆-alkynyl moieties of(C₁-C₆-alkoxy)-C₂-C₆-alkynyl: linear or branched unsaturated hydrocarbongroup having 2 to 6 carbon atoms and containing at least one C—C-triplebond, such as ethynyl, 1-propynyl, 2-propynyl (propargyl), 1-butynyl,2-butynyl, 3-butynyl, 1-methyl-2-propynyl and the like; C₁-C₄-haloalkyl:a C₁-C₄-alkyl radical as mentioned above which is partially or fullysubstituted by fluorine, chlorine, bromine and/or iodine, for example,chloro-methyl, dichloromethyl, trichloromethyl, fluoromethyl,difluoromethyl, trifluoromethyl, chlorofluoromethyl,dichlorofluoromethyl, chlorodifluoromethyl, bromomethyl, iodomethyl,2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl,2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl,2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl,2,2,2-trichloroethyl, pentafluoroethyl, 2-fluoropropyl, 3-fluoropropyl,2,2-difluoropropyl, 2,3-difluoropropyl, 2-chloropropyl, 3-chloropropyl,2,3-dichloropropyl, 2-bromopropyl, 3-bromopropyl, 3,3,3-trifluoropropyl,3,3,3-trichloropropyl, 2,2,3,3,3-pentafluoropropyl, heptafluoropropyl,1-(fluoromethyl)-2-fluoroethyl, 1-(chloromethyl)-2-chloroethyl,1-(bromomethyl)-2-bromoethyl, 4-fluorobutyl, 4-chlorobutyl,4-bromobutyl, nonafluorobutyl, 1,1,2,2,-tetrafluoroethyl and1-trifluoromethyl-1,2,2,2-tetrafluoroethyl;

C₁-C₆-haloalkyl: C₁-C₄-haloalkyl as mentioned above, and also, forexample, 5-fluoropentyl, 5-chloropentyl, 5-bromopentyl, 5-iodopentyl,undecafluoropentyl, 6-fluorohexyl, 6-chlorohexyl, 6-bromohexyl,6-iodohexyl and dodecafluorohexyl; C₃-C₆-cycloalkyl: monocyclicsaturated hydrocarbons having 3 to 6 ring members, such as cyclopropyl,cyclobutyl, cyclopentyl and cyclohexyl;

C₁-C₄-alkoxy: for example methoxy, ethoxy, propoxy, 1-methylethoxybutoxy, 1-methylpropoxy, 2-methylpropoxy and 1,1-dimethylethoxy;

C₁-C₆-alkoxy and also the C₁-C₆-alkoxy moieties of(C₁-C₆-alkoxy)carbonyl, (C₁-C₆-alkoxy)sulfonyl,(C₁-C₆-alkoxy)-C₁-C₆-alkyl: C₁-C₄-alkoxy as mentioned above, and also,for example, pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methoxylbutoxy,1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy,1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy,3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy,1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy,2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy,1,1,2-trimethylpropoxy, 1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxyand 1-ethyl-2-methylpropoxy;

C₁-C₄-haloalkoxy: a C₁-C₄-alkoxy radical as mentioned above which ispartially or fully substituted by fluorine, chlorine, bromine and/oriodine, for example, chloro-methoxy, dichloromethoxy, trichloromethoxy,fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorofluoromethoxy,dichlorofluoromethoxy, chlorodifluoromethoxy2-fluoroethoxy,2-chloroethoxy, 2-bromoethxoy, 2,2-difluoroethoxy,2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy,2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy,2,2,2-trichloroethoxy, pentafluoroethoxy, 2-fluoropropoxy,3-fluoropropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy,2-chloropropoxy, 3-chloropropoxy, 2,3-dichloropropoxy,3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy,2,2,3,3,3-pentafluoropropoxy, heptafluoropropoxy,1-(fluoromethyl)-2-fluoroethoxy, 4-fluorobutoxy, nonafluorobutoxy,1,1,2,2,-tetrafluoroethoxy and1-trifluoromethyl-1,2,2,2-tetrafluoroethoxy;

C₁-C₄-alkylthio: for example methylthio, ethylthio, propylthio,1-methylethylthio, butylthio, 1-methylpropylthio, 2-methylpropylthio and1,1-dimethylethylthio;

C₁-C₆-alkylthio: C₁-C₄-alkylthio as mentioned above, and also, forexample, pentylthio, 1-methylbutylthio, 2-methylbutylthio,3-methylbutylthio, 2,2-dimethylpropylthio, 1-ethylpropylthio, hexylthio,1,1-dimethylpropylthio, 1,2-dimethylpropylthio, 1-methylpentylthio,2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio,1,1-dimethylbutylthio, 1,2-dimethylbutylthio, 1,3-dimethylbutylthio,2,2-dimethylbutylthio, 2,3-dimethylbutylthio, 3,3-dimethylbutylthio,1-ethylbutylthio, 2-ethylbutylthio, 1,1,2-trimethylpropylthio,1,2,2-trimethylpropylthio, 1-ethyl-1-methylpropylthio and1-ethyl-2-methylpropylthio;

C₁-C₆-haloalkylthio: a C₁-C₆-alkylthio radical as mentioned above whichis partially or fully substituted by fluorine, chlorine, bromine and/oriodine, for example, chloro-methoxy, dichloromethoxy, trichloromethoxy,fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorofluoromethoxy,dichlorofluoromethoxy, chlorodifluoromethoxy2-fluoroethoxy,2-chloroethoxy, 2-bromoethxoy, 2,2-difluoroethoxy,2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy,2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy,2,2,2-trichloroethoxy, pentafluoroethoxy, 2-fluoropropoxy,3-fluoropropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy,2-chloropropoxy, 3-chloropropoxy, 2,3-dichloropropoxy,3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy,2,2,3,3,3-pentafluoropropoxy, heptafluoropropoxy,1-(fluoromethyl)-2-fluoroethoxy, 4-fluorobutoxy, nonafluorobutoxy,1,1,2,2,-tetrafluoroethoxy and1-trifluoromethyl-1,2,2,2-tetrafluoroethoxy;

C₁-C₆-alkylsulfinyl (C₁-C₆-alkyl-S(═O)—): e.g. methylsulfinyl,ethylsulfinyl, propylsulfinyl, 1-methylethylsulfinyl, butylsulfinyl,1-methylpropylsulfinyl, 2-methylpropylsulfinyl,1,1-dimethylethylsulfinyl, pentylsulfinyl, 1-methylbutylsulfinyl,2-methylbutylsulfinyl, 3-methylbutylsulfinyl,2,2-dimethylpropylsulfinyl, 1-ethylpropylsulfinyl,1,1-dimethylpropylsulfinyl, 1,2-dimethylpropylsulfinyl, hexylsulfinyl,1-methylpentylsulfinyl, 2-methylpentylsulfinyl, 3-methylpentylsulfinyl,4-methylpentyl-sulfinyl, 1,1-dimethylbutylsulfinyl,1,2-dimethylbutylsulfinyl, 1,3-dimethylbutyl-sulfinyl,2,2-dimethylbutylsulfinyl, 2,3-dimethylbutylsulfinyl,3,3-dimethylbutyl-sulfinyl, 1-ethylbutylsulfinyl, 2-ethylbutylsulfinyl,1,1,2-trimethylpropylsulfinyl, 1,2,2-trimethylpropylsulfinyl,1-ethyl-1-methylpropylsulfinyl and 1-ethyl-2-methylpropylsulfinyl;

C₁-C₆-haloalkylsulfinyl (C₁-C₆-alkyl-S(═O)—): a C₁-C₆-alkylsulfinylradical as mentioned above which is partially or fully substituted byfluorine, chlorine, bromine and/or iodine, for example, chloro-methoxy,dichloromethoxy, trichloromethoxy, fluoromethoxy, difluoromethoxy,trifluoromethoxy, chlorofluoromethoxy, dichlorofluoromethoxy,chlorodifluoromethoxy2-fluoroethoxy, 2-chloroethoxy, 2-bromoethxoy,2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy,2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy,2,2,2-trichloroethoxy, pentafluoroethoxy, 2-fluoropropoxy,3-fluoropropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy,2-chloropropoxy, 3-chloropropoxy, 2,3-dichloropropoxy,3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy,2,2,3,3,3-pentafluoropropoxy, heptafluoropropoxy,1-(fluoromethyl)-2-fluoroethoxy, 4-fluorobutoxy, nonafluorobutoxy,1,1,2,2,-tetrafluoroethoxy and1-trifluoromethyl-1,2,2,2-tetrafluoroethoxy;

C₁-C₆-alkylsulfonyl (C₁-C₆-alkyl-S(O)₂—): for example methylsulfonyl,ethylsulfonyl, propylsulfonyl, 1-methylethylsulfonyl, butylsulfonyl,1-methylpropylsulfonyl, 2-methyl-propylsulfonyl,1,1-dimethylethylsulfonyl, pentylsulfonyl, 1-methylbutylsulfonyl,2-methylbutylsulfonyl, 3-methylbutylsulfonyl,1,1-dimethylpropylsulfonyl, 1,2-dimethylpropylsulfonyl,2,2-dimethylpropylsulfonyl, 1-ethylpropylsulfonyl, hexylsulfonyl,1-methylpentylsulfonyl, 2-methylpentylsulfonyl, 3-methylpentylsulfonyl,4-methylpentylsulfonyl, 1,1-dimethylbutylsulfonyl,1,2-dimethylbutylsulfonyl, 1,3-dimethylbutylsulfonyl,2,2-dimethylbutylsulfonyl, 2,3-dimethylbutylsulfonyl,3,3-dimethylbutylsulfonyl, 1-ethylbutylsulfonyl, 2-ethylbutylsulfonyl,1,1,2-trimethyl-propylsulfonyl, 1,2,2-trimethylpropylsulfonyl,1-ethyl-1-methylpropylsulfonyl and 1-ethyl-2-methylpropylsulfonyl;

C₁-C₆-haloalkylsulfonyl (C₁-C₆-alkyl-S(O)₂—): C₁-C₆-alkylsulfonylradical as mentioned above which is partially or fully substituted byfluorine, chlorine, bromine and/or iodine, for example, chloro-methoxy,dichloromethoxy, trichloromethoxy, fluoromethoxy, difluoromethoxy,trifluoromethoxy, chlorofluoromethoxy, dichlorofluoromethoxy,chlorodifluoromethoxy2-fluoroethoxy, 2-chloroethoxy, 2-bromoethxoy,2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy,2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy,2,2,2-trichloroethoxy, pentafluoroethoxy, 2-fluoropropoxy,3-fluoropropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy,2-chloropropoxy, 3-chloropropoxy, 2,3-dichloropropoxy,3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy,2,2,3,3,3-pentafluoropropoxy, heptafluoropropoxy,1-(fluoromethyl)-2-fluoroethoxy, 4-fluorobutoxy, nonafluorobutoxy,1,1,2,2,-tetrafluoroethoxy and1-trifluoromethyl-1,2,2,2-tetrafluoroethoxy;

(C₁-C₄-alkyl)amino and also the (C₁-C₄-alkylamino) moieties of(C₁-C₄-alkylamino)carbonyl or (C₁-C₄-alkylamino)sulfonyl: for examplemethylamino, ethylamino, propylamino, 1-methylethylamino, butylamino,1-methylpropylamino, 2-methylpropylamino or 1,1-dimethylethylamino;

(C₁-C₆-alkyl)amino and also the (C₁-C₆-alkylamino) moieties of(C₁-C₆-alkylamino)carbonyl or (C₁-C₆-alkylamino)sulfonyl:(C₁-C₄-alkyl)amino as mentioned above, and also, for example,pentylamino, 1-methylbutylamino, 2-methylbutylamino, 3-methylbutylamino,2,2-dimethylpropylamino, 1-ethylpropylamino, hexylamino,1,1-dimethylpropylamino, 1,2-dimethylpropylamino, 1-methylpentylamino,2-methylpentylamino, 3-methylpentylamino, 4-methylpentylamino,1,1-dimethylbutylamino, 1,2-dimethylbutylamino, 1,3-dimethylbutylamino,2,2-dimethylbutylamino, 2,3-dimethylbutyl-amino 3,3-dimethylbutylamino,1-ethylbutylamino, 2-ethylbutylamino, 1,1,2-trimethylpropylamino,1,2,2-trimethyl-propylamino, 1-ethyl-1-methylpropylamino or1-ethyl-2-methylpropylamino;

di(C₁-C₄-alkyl)amino and also the di(C₁-C₄-alkylamino) moieties ofdi(C₁-C₄-alkylamino)carbonyl or di(C₁-C₄-alkylamino)sulfonyl: forexample N,N-dimethylamino, N,N-diethylamino, N,N-di(1-methylethyl)amino,N,N-dipropylamino, N,N-dibutylamino, N,N-di(1-methylpropyl)amino,N,N-di(2-methylpropyl)amino, N,N-di(1,1-dimethylethyl)amino,N-ethyl-N-methylamino, N-methyl-N-propylamino,N-methyl-N-(1-methylethyl)amino, N-butyl-N-methylamino,N-methyl-N-(1-methylpropyl)amino, N-methyl-N-(2-methylpropyl)amino,N-(1,1-dimethylethyl)-N-methylamino, N-ethyl-N-propylamino,N-ethyl-N-(1-methylethyl)amino, N-butyl-N-ethylamino,N-ethyl-N-(1-methylpropyl)amino, N-ethyl-N-(2-methylpropyl)amino,N-ethyl-N-(1,1-dimethylethyl)amino, N-(1-methylethyl)-N-propylamino,N-butyl-N-propylamino, N-(1-methylpropyl)-N-propylamino,N-(2-methylpropyl)-N-propylamino, N-(1,1-dimethylethyl)-N-propylamino,N-butyl-N-(1-methylethyl)amino,N-(1-methylethyl)-N-(1-methylpropyl)amino,N-(1-methylethyl)-N-(2-methylpropyl)amino,N-(1,1-dimethylethyl)-N-(1-methylethyl)amino,N-butyl-N-(1-methylpropyl)amino, N-butyl-N-(2-methylpropyl)amino,N-butyl-N-(1,1-dimethylethyl)amino,N-(1-methylpropyl)-N-(2-methylpropyl)amino,N-(1,1-dimethylethyl)-N-(1-methylpropyl)amino or N-(1,1-dimethylethyl)-N-(2-methylpropyl)amino;

di(C₁-C₆-alkyl)amino and also the di(C₁-C₆-alkylamino) moieties ofdi(C₁-C₆-alkylamino)carbonyl or di(C₁-C₆-alkylamino)sulfonyl:di(C₁-C₄-alkyl)amino as mentioned above, and also, for example,N-methyl-N-pentylamino, N-methyl-N-(1-methylbutyl)amino,N-methyl-N-(2-methylbutyl)amino, N-methyl-N-(3-methylbutyl)amino,N-methyl-N-(2,2-dimethylpropyl)amino, N-methyl-N-(1-ethylpropyl)amino,N-methyl-N-hexylamino, N-methyl-N-(1,1-dimethylpropyl)amino,N-methyl-N-(1,2-dimethylpropyl)amino, N-methyl-N-(1-methylpentyl)amino,N-methyl-N-(2-methylpentyl)amino, N-methyl-N-(3-methylpentyl)amino,N-methyl-N-(4-methylpentyl)amino, N-methyl-N-(1,1-dimethylbutyl)amino,N-methyl-N-(1,2-dimethylbutyl)amino,N-methyl-N-(1,3-dimethylbutyl)amino,N-methyl-N-(2,2-dimethylbutyl)amino,N-methyl-N-(2,3-dimethylbutyl)amino,N-methyl-N-(3,3-dimethylbutyl)amino, N-methyl-N-(1-ethylbutyl)amino,N-methyl-N-(2-ethylbutyl)amino, N-methyl-N-(1,1,2-trimethylpropyl)amino,N-methyl-N-(1,2,2-trimethylpropyl)amino,N-methyl-N-(1-ethyl-1-methylpropyl)amino,N-methyl-N-(1-ethyl-2-methylpropyl)amino, N-ethyl-N-pentylamino,N-ethyl-N-(1-methylbutyl)amino, N-ethyl-N-(2-methylbutyl)amino,N-ethyl-N-(3-methylbutyl)amino, N-ethyl-N-(2,2-dimethylpropyl)amino,N-ethyl-N-(1-ethylpropyl)amino, N-ethyl-N-hexylamino,N-ethyl-N-(1,1-dimethylpropyl)amino,N-ethyl-N-(1,2-dimethylpropyl)amino, N-ethyl-N-(1-methylpentyl)amino,N-ethyl-N-(2-methylpentyl)amino, N-ethyl-N-(3-methylpentyl)amino,N-ethyl-N-(4-methylpentyl)amino, N-ethyl-N-(1,1-dimethylbutyl)amino,N-ethyl-N-(1,2-dimethylbutyl)amino, N-ethyl-N-(1,3-dimethylbutyl)amino,N-ethyl-N-(2,2-dimethylbutyl)amino, N-ethyl-N-(2,3-dimethylbutyl)amino,N-ethyl-N-(3,3-dimethylbutyl)amino, N-ethyl-N-(1-ethylbutyl)amino,N-ethyl-N-(2-ethylbutyl)amino, N-ethyl-N-(1,1,2-trimethylpropyl)amino,N-ethyl-N-(1,2,2-trimethylpropyl)amino,N-ethyl-N-(1-ethyl-1-methylpropyl)amino,N-ethyl-N-(1-ethyl-2-methylpropyl)amino, N-propyl-N-pentylamino,N-butyl-N-pentylamino, N,N-dipentylamino, N-propyl-N-hexylamino,N-butyl-N-hexylamino, N-pentyl-N-hexylamino or N,N-dihexylamino;

C₃-C₆-cyclolalkyl and also the C₃-C₆-cyclolalkyl moieties of(C₃-C₆-cyclolalkyl)-carbonyl, (C₃-C₆-cyclolalkyl)-C₁-C₆-alkyl and(C₃-C₆-cyclolalkyl)-C₁-C₆-alkoxy: a cycloaliphatic radical having 3 to 6carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl andcyclohexyl;

C₃-C₆-halocycloalkyl: is also expressed as “cycloalkyl which ispartially or fully halogenated”, refers C₃-C₆-cycloalkyl as mentionedabove, in which some or all of the hydrogen atoms are replaced byhalogen atoms as mentioned above, in particular fluorine, chlorine andbromine. Examples of C₃-C₆-halocycloalkyl include 1-fluorocycloprpyl,2-fluorocyclopropyl, 2,2-difluorocyclopropyl, 1-chlorocyclcopropyl,2-chlorocyclopropyl, 2,2-dichlorocyclopropyl, 2,3-difluorocyclopropyl,1-fluorocycobutyl etc.;

C₃-C₆-halocycloalkyl-C₁-C₄-alkyl: refers to a C₃-C₆-halocycloalkyl groupas defined above which is bound to the remainder of the molecule via aC₁-C₄-alkyl group, as defined above;

C₁-C₆-cycloalkoxy: C₁-C₆-cycloakyl as mentioned above, which is bound tothe remainder of the molecule by an oxygen atom;

C₁-C₆-halocycloalkoxy: C₁-C₆-halocycloaklyl as mentioned above, which isbound to the remainder of the molecule by a oxygen atom

(C₁-C₆-cycloalkyl)-C₁-C₆-alkoxy: C₁-C₆-alkoxy as mentioned above wherein1 hydrogen atom is replaced by C₃-C₆-cyclolalkyl as defined above;

(C₁-C₆-halocycloalkyl)-C₁-C₆-alkoxy: C₁-C₆-alkoxy as mentioned abovewherein 1 hydrogen atom is replaced by C₃-C₆-halocyclolalkyl as definedabove;

(C₁-C₆-cycloalkoxy)-C₁-C₆-alkyl: C₁-C₆-alkyl as mentioned above wherein1 hydrogen atom is replaced by C₃-C₆-cyclolalkoxy as defined above;

(C₁-C₆-cycloalkyl)-carbonyl: C₁-C₆-cycloalkyl as mentioned above whichis bound to the remainder of the molecule by a carbonyl group;

C₃-C₆-cycloalkan-1,1-diyl, e.g. cyclopropan-1,1-diyl,cyclobutan-1,1-diyl, cyclopentan-1,1-diyl or cyclohexan-1,1-diyl;

ipso-C₃-C₆-cycloalkendiyl: ipso-connected bivalent unsaturatedcycloaliphatic radical having 3 to 6-carbon atoms as ring members, e.g.cyclobuten-3,3-diyl, cyclobuten-4,4-diyl, cyclopenten-3,3-diyl,cyclopenten-4,4-diyl, cyclopenten-5,5-diyl, cyclohexen-3,3-diyl,cyclohexen-4,4-diyl, cyclohexen-5,5-diyl or cyclohexen-6,6-diyl.

(C₃-C₆-cyclolalkyl)-C₁-C₆-alkyl: C₁-C₆-alkyl, in particular C₁-C₄-alkylas defined above, such as methyl or ethyl, wherein 1 hydrogen atom isreplaced by C₃-C₆-cyclolalkyl as defined above, examples includingcyclopropylmethyl (CH₂-cyclopropyl), cyclobutylmethyl,cyclopentylmethyl, cycloexylmethyl, 1-cyclopropylethyl(CH(CH₃)-cyclopropyl), 1-cyclobutylethyl, 1-cyclopentylethyl,1-cycloexylethyl, 2-cyclopropylethyl (CH₂CH₂-cyclopropyl),2-cyclobutylethyl, 2-cyclopentylethyl or 2-cycloexylethyl;

(C₁-C₆-alkoxy)-C₁-C₆-alkyl: C₁-C₆-alkyl, in particular C₁-C₄-alkyl asdefined above, such as methyl, ethyl or isopropyl, wherein 1 hydrogenatom is replaced by C₁-C₆-alkoxy as defined above, examples includingmethoxymethyl, ethoxymethyl, n-propoxymethyl, butoxymethyl,1-methoxyethyl, 1-ethoxyethyl, 1-(n-propoxy)ethyl, 1-butoxyethyl,2-methoxyethyl, 2-ethoxyethyl, 2-(n-propoxy)ethyl, 2-butoxyethyl,2-methoxypropyl, 2-ethoxypropyl, 2-(n-propoxy)propyl, 2-butoxypropyl;

(C₁-C₆-alkoxy)-C₁-C₆-alkoxy: C₁-C₆-alkoxy, in particular C₁-C₄-alkoxy asdefined above, wherein 1 hydrogen atom is replaced by C₁-C₆-alkoxy asdefined above;

(C₁-C₆-haloalkoxy)-C₁-C₆-alkoxy: C₁-C₆-alkoxy, in particularC₁-C₄-alkoxy as defined above, wherein 1 hydrogen atom is replaced byC₁-C₆-haloalkoxy as defined above;

(C₁-C₆-alkyl)carbonyl: C₁-C₆-alkyl as mentioned above, which is bound tothe remainder of the molecule by a carbonyl group;

(C₁-C₆-haloalkyl)-carbonyl: C₁-C₆-haloalkyl as mentioned above, which isbound to the remainder of the molecule by a carbonyl group;

(C₁-C₆-alkoxy)carbonyl: C₁-C₆-alkyloxy as mentioned above, which isbound to the remainder of the molecule by a carbonyl group;

(C₁-C₆-alkylamino)carbonyl: (C₁-C₆-alkyl)amino as mentioned above, whichis bound to the remainder of the molecule by a carbonyl group;

(C₁-C₆-alkylamino)sulfonyl: (C₁-C₆-alkyl)amino as mentioned above, whichis bound to the remainder of the molecule by a sulfonyl group;

di(C₁-C₆-alkylamino)carbonyl: di(C₁-C₆-alkyl)amino as mentioned above,which is bound to the remainder of the molecule by a carbonyl group;

di(C₁-C₆-alkylamino)sulfonyl: di(C₁-C₆-alkyl)amino as mentioned above,which is bound to the remainder of the molecule by a sulfonyl group;

phenyl-C₁-C₆-alkyl: C₁-C₆-alkyl, in particular C₁-C₄-alkyl as definedabove, such as methyl or ethyl, wherein 1 hydrogen atom is replaced byphenyl, examples including benzyl, 1-phenylethyl, 2-phenylethyl,1-phenylpropyl, 2-phenylpropyl, 1-phenyl-1-methylethyl etc.;

three- to six-membered saturated or partially unsaturatedipso-heterocyclodiyl is an ipso-connected bivalent heterocyclic radical,which is saturated or unsaturated, which has 3 to 6 ring atoms, whereinat least 1 ring atom, e.g. 1, 2 or 3 ring atoms are selected from O, Sand N, examples being oxiran-2,2-diyl, oxetan-2,2-diyl, oxetan-3,3-diyl,oxolan-2,2-diyl, oxolan-3,3-diyl, 1,3-dioxolan-2,2-diyl, oxan-2,2-diyl,oxan-3,3-diyl or oxan-4,4-diyl, 1,3-dioxan-2,2-diyl, thiolan-2,2-diyl,thiolan-3,3-diyl, pyrrolidin-2,2-diyl, pyrroldin-3,3-diyl,piperidin-2,2,-diyl, piperidin-3,3-diyl, piperidin-4,4-diyl.

The preferred embodiments of the invention mentioned herein below haveto be understood as being preferred either independently from each otheror in combination with one another. Particular groups of embodiments ofthe invention relate to those diaminotriazines of formula (I), whereinthe variables R^(a), R^(b), q, R¹, R², R³, R⁴ and R⁵, eitherindependently of one another or in combination with one another, havethe following meanings:

Particular groups of embodiments relate to the diaminotriazine compoundsof formula (I), wherein

-   R^(a) is selected from the group consisting of C₁-C₆-haloalkoxy,    C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy,    C₂-C₆-haloalkynyloxy, (C₁-C₆-alkoxy)-C₁-C₆-alkoxy,    C₃-C₆-cycloalkoxy, C₃-C₆-halocycloalkoxy,    (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy and    (C₃-C₆-halocycloalkyl)-C₁-C₄-alkoxy, in particular selected from the    group consisting of C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy,    C₃-C₆-cycloalkoxy, C₃-C₆-halocycloalkoxy,    (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy and    (C₃-C₆-halocycloalkyl)-C₁-C₄-alkoxy, more particularly from the    group consisting of C₂-C₄-alkynyloxy, such as 2-propynyloxy    (=propargyloxy), C₂-C₄-alkenyloxy, such as 2-propenyloxy    (=allyloxy), C₃-C₆-cycloalkoxy, such as cyclopropyloxy,    cyclobutyloxy, cyclopentyloxy and cyclohexyloxy, and    (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy, in particular    (C₃-C₆-cycloalkyl)-C₁-C₂-alkoxy, such as cyclopropylmethoxy,    cyclobutylmethoxy, cyclopentylmethoxy and cyclohexylmethoxy;-   R^(b) is as defined above, in particular selected from the group    consisting of halogen, CN, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,    C₃-C₆-cycloalkoxy and C₃-C₆-halocycloalkoxy, more particularly    selected from the group consisting of halogen, such as fluorine,    chlorine or bromine, CN, C₁-C₄-alkoxy, such as methoxy or ethoxy,    and C₁-C₄-haloalkoxy, such as difluoromethoxy, trifluoromethoxy,    1,1-difluoroethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy    and pentafluoroethoxy, even more particularly from fluorine and    C₁-C₄-alkoxy, especially is fluorine; wherein in case the variable q    is 2 or 3 the two or three radicals R^(b) may be identical or    different;-   q is 0, 1, 2 or 3, in particular 0, 1 or 2.

Further particular groups of embodiments relate to the diaminotriazinecompounds of formula (I), wherein

-   R^(a) is selected from the group consisting of C₂-C₆-alkenyloxy,    C₂-C₆-alkynyloxy, C₃-C₆-cycloalkoxy, C₃-C₆-halocycloalkoxy,    (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy and    (C₃-C₆-halocycloalkyl)-C₁-C₄-alkoxy, in particular from from    C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy, C₃-C₆-cycloalkoxy and    (C₃-C₆-cycloalkyl)-C₁-C₂-alkoxy, especially from the group    consisting of C₃-C₆-cycloalkoxy, such as cyclopropyloxy,    cyclobutyloxy, cyclopentyloxy and cyclohexyloxy, and    (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy, in particular    (C₃-C₆-cycloalkyl)-C₁-C₂-alkoxy, such as cyclopropylmethoxy,    cyclobutylmethoxy, cyclopentylmethoxy and cyclohexylmethoxy;-   R^(b) is selected from the group consisting of halogen, CN,    C₁-C₄-alkoxy and C₁-C₄-haloalkoxy, more particularly from fluorine    and C₁-C₄-alkoxy, especially is fluorine;-   q is 0, 1 or 2, in particular 0 or 1.

Special groups of embodiments relate to the diaminotriazine compounds offormula (I), wherein

-   R^(a) is C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy, C₃-C₆-cycloalkoxy or    (C₃-C₆-cycloalkyl)-C₁-C₂-alkoxy, in particular prop-2-enoxy,    prop-2-ynoxy, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy,    cyclohexyloxy, (cyclopropyl)methyloxy, (cyclobutyl)methyloxy,    (cyclopentyl)methyloxy or (cyclohexyl)methyloxy;-   R^(b) is fluorine, methoxy, ethoxy, n-propoxy, 2-propoxy, n-butoxy,    2-butoxy, 2-methyl-1-propoxy or tert.-butoxy, especially fluorine;-   q is 0 or 1, in particular 0.

In particular embodiments of the invention, the following moiety of theformula (A) included in the diaminotriazine compounds of formula (I)

is represented by the moiety

wherein R^(a) has the herein defined meanings, in particular thosemeanings mentioned herein as preferred, more particularly from the groupconsisting of C₂-C₄-alkynyloxy, such as 2-propynyloxy (=propargyloxy),C₂-C₄-alkenyloxy, such as 2-propenyloxy (=allyloxy), C₃-C₆-cycloalkoxy,such as cyclopropyloxy, cyclobutyloxy, cyclopentyloxy and cyclohexyloxy,and (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy, in particular(C₃-C₆-cycloalkyl)-C₁-C₂-alkoxy, such as cyclopropylmethoxy,cyclobutylmethoxy, cyclopentylmethoxy and cyclohexylmethoxy; and R^(b1),R^(b2) and R^(b3) are identical or different and are hydrogen or haveone of the meanings of R^(b) defined herein, in particular thosemeanings mentioned herein as preferred. According to preferredembodiments of the invention R^(b1), R^(b2) and R^(b3) are independentlyselected from the group consisting of hydrogen, halogen, CN,C₁-C₄-alkoxy and C₁-C₄-haloalkoxy, more particularly from hydrogen,fluorine and C₁-C₄-alkoxy, especially from hydrogen and fluorine.

In particular embodiments of the invention, the moiety of the formula(A)

is selected from the group consisting of2-fluoro-6-(cyclopropyloxy)phenyl, 2-fluoro-6-(cyclobutyloxy)phenyl,2-fluoro-6-(cyclopentyloxy)phenyl, 2-fluoro-6-(cyclohexyloxy)phenyl,2-fluoro-6-[(cyclopropyl)methyloxy]phenyl,2-fluoro-6-[(cyclobutyl)methyloxy]phenyl,2-fluoro-6-[(cyclopentyl)methyloxy]phenyl,2-fluoro-6-[(cyclohexyl)methyloxy]phenyl, 2-fluoro-6-prop-2-enoxyphenyl,2-fluoro-6-prop-2-ynoxyphenyl, 2,3-difluoro-6-(cyclopropyloxy)phenyl,2,3-difluoro-6-(cyclobutyloxy)phenyl,2,3-difluoro-6-(cyclopentyloxy)phenyl,2,3-difluoro-6-(cyclohexyloxy)phenyl,2,3-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3-difluoro-6-prop-2-enoxyphenyl, 2,3-difluoro-6-prop-2-ynoxyphenyl,2,4-difluoro-6-(cyclopropyloxy)phenyl,2,4-difluoro-6-(cyclobutyloxy)phenyl,2,4-difluoro-6-(cyclopentyloxy)phenyl,2,4-difluoro-6-(cyclohexyloxy)phenyl,2,4-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,4-difluoro-6-prop-2-enoxyphenyl, 2,4-difluoro-6-prop-2-ynoxyphenyl,2,5-difluoro-6-(cyclopropyloxy)phenyl,2,5-difluoro-6-(cyclobutyloxy)phenyl,2,5-difluoro-6-(cyclopentyloxy)phenyl,2,5-difluoro-6-(cyclohexyloxy)phenyl,2,5-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,5-difluoro-6-prop-2-enoxyphenyl, 2,5-difluoro-6-prop-2-ynoxyphenyl,2,3,5-trifluoro-6-(cyclopropyloxy)phenyl,2,3,5-trifluoro-6-(cyclobutyloxy)phenyl,2,3,5-trifluoro-6-(cyclopentyloxy)phenyl,2,3,5-trifluoro-6-(cyclohexyloxy)phenyl,2,3,5-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,5-trifluoro-6-prop-2-enoxyphenyl,2,3,5-trifluoro-6-prop-2-ynoxyphenyl,2,4,5-trifluoro-6-(cyclopropyloxy)phenyl,2,4,5-trifluoro-6-(cyclobutyloxy)phenyl,2,4,5-trifluoro-6-(cyclopentyloxy)phenyl,2,4,5-trifluoro-6-(cyclohexyloxy)phenyl,2,4,5-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclobutyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,4,5-trifluoro-6-prop-2-enoxyphenyl,2,4,5-trifluoro-6-prop-2-ynoxyphenyl,2,3,4-trifluoro-6-(cyclopropyloxy)phenyl,2,3,4-trifluoro-6-(cyclobutyloxy)phenyl,2,3,4-trifluoro-6-(cyclopentyloxy)phenyl,2,3,4-trifluoro-6-(cyclohexyloxy)phenyl,2,3,4-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,4-trifluoro-6-prop-2-enoxyphenyl,2,3,4-trifluoro-6-prop-2-ynoxyphenyl,2,3,4,5-tretrafluoro-6-(cyclopropyloxy)phenyl,2,3,4,5-tretrafluoro-6-(cyclobutyloxy)phenyl,2,3,4,5-tretrafluoro-6-(cyclopentyloxy)phenyl,2,3,4,5-tretrafluoro-6-(cyclohexyloxy)phenyl,2,3,4,5-tretrafluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,4,5-tretrafluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3,4,5-tretrafluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,4,5-tretrafluoro-6-[(cyclohexyl)methyloxy]-phenyl,2,3,4,5-tretrafluoro-6-prop-2-enoxyphenyl and2,3,4,5-tretrafluoro-6-prop-2-ynoxyphenyl;

with preference given to 2-fluoro-6-(cyclopropyloxy)phenyl,2-fluoro-6-(cyclobutyloxy)phenyl, 2-fluoro-6-(cyclopentyloxy)phenyl,2-fluoro-6-(cyclohexyloxy)phenyl,2-fluoro-6-[(cyclopropyl)methyloxy]phenyl,2-fluoro-6-[(cyclobutyl)methyloxy]phenyl,2-fluoro-6-[(cyclopentyl)methyloxy]phenyl,2-fluoro-6-[(cyclohexyl)methyloxy]phenyl, 2-fluoro-6-prop-2-enoxyphenyl,2-fluoro-6-prop-2-ynoxyphenyl, 2,3-difluoro-6-(cyclopropyloxy)phenyl,2,3-difluoro-6-(cyclopentyloxy)phenyl,2,3-difluoro-6-(cyclohexyloxy)phenyl,2,3-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,4-difluoro-6-(cyclopropyloxy)phenyl,2,4-difluoro-6-(cyclopentyloxy)phenyl,2,4-difluoro-6-(cyclohexyloxy)phenyl,2,4-difluoro-6-[(cyclopropyl)-methyloxy]phenyl,2,4-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,5-difluoro-6-(cyclopropyloxy)phenyl,2,5-difluoro-6-(cyclopentyloxy)phenyl,2,5-difluoro-6-(cyclohexyloxy)phenyl,2,5-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,5-trifluoro-6-(cyclopropyloxy)phenyl,2,3,5-trifluoro-6-(cyclopentyloxy)phenyl,2,3,5-trifluoro-6-(cyclohexyloxy)phenyl,2,3,5-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,4,5-trifluoro-6-(cyclopropyloxy)phenyl,2,4,5-trifluoro-6-(cyclopentyloxy)phenyl,2,4,5-trifluoro-6-(cyclohexyloxy)phenyl,2,4,5-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,4-trifluoro-6-(cyclopropyloxy)phenyl,2,3,4-trifluoro-6-(cyclopentyloxy)phenyl,2,3,4-trifluoro-6-(cyclohexyloxy)phenyl,2,3,4-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,4,5-tretrafluoro-6-(cyclopropyloxy)phenyl,2,3,4,5-tretrafluoro-6-(cyclopentyloxy)phenyl,2,3,4,5-tretrafluoro-6-(cyclohexyloxy)phenyl,2,3,4,5-tretrafluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,4,5-tretrafluoro-6-[(cyclopentyl)methyloxy]phenyl and2,3,4,5-tretrafluoro-6-[(cyclohexyl)methyloxy]phenyl.

Particular groups of embodiments relate to the diaminotriazine compoundsof formula (I), wherein;

-   R¹ is H, CN, C₁-C₆-alkyl, (C₁-C₆-alkoxy)-C₁-C₆-alkyl,    (C₁-C₆-alkyl)carbonyl, (C₃-C₆-cycloalkyl)carbonyl,    (C₁-C₆-alkyl)sulfonyl, C₁-C₆-alkoxy, (C₁-C₆-alkoxy)carbonyl,    (C₁-C₆-alkylamino)carbonyl, di(C₁-C₆-alkyl)aminocarbonyl,    (C₁-C₆-alkylamino)sulfonyl, di(C₁-C₆-alkyl)aminosulfonyl, where the    aliphatic parts of the 11 aforementioned radicals are unsubstituted,    partly or completely halogenated,    -   phenyl, phenylcarbonyl and phenyl-C₁-C₆-alkyl,    -   wherein phenyl in the last 3 mentioned radical is unsubstituted        or substituted by 1, 2, 3, 4, or 5 identical or different        substituents selected from the group consisting of halogen, CN,        NO₂, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy and        C₁-C₆-haloalkoxy; preferably R¹ is H, CN, C₁-C₆-alkyl,        (C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkyl)carbonyl,        (C₃-C₆-cycloalkyl)carbonyl, C₁-C₆-alkoxy or        (C₁-C₆-alkyl)sulfonyl, where the aliphatic parts of the 6        aforementioned radicals unsubstituted partly or completely        halogenated, phenyl and phenyl-C₁-C₆ alkyl,    -   wherein phenyl in the last 2 mentioned radical is unsubstituted        or substituted by 1, 2, 3, 4, or 5 identical or different        substituents selected from the group consisting of halogen, CN,        NO₂, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy and        C₁-C₆-haloalkoxy; in particular R¹ is H, CN, C₁-C₆-alkyl,        C₁-C₆-haloalkyl, (C₁-C₆-alkoxy)-C₁-C₆-alkyl, C₁-C₆-alkoxy,        (C₁-C₆-alkyl)carbonyl, (C₃-C₆-cycloalkyl)carbonyl,        (C₁-C₆-haloalkyl)carbonyl, (C₁-C₆-alkyl)sulfonyl or        (C₁-C₆-haloalkyl)sulfonyl;    -   more particularly R¹ is H, CN, C₁-C₄-alkyl,        (C₁-C₄-alkoxy)-C₁-C₄-alkyl, C₁-C₄-alkoxy, (C₁-C₄-alkyl)carbonyl,        (C₃-C₅-cycloalkyl)carbonyl or (C₁-C₄-alkyl)sulfonyl; even more        particularly H, CN, CH₃, CH₂OCH₃, OCH₃, C(O)CH₃,        cyclopropyl-carbonyl or SO₂CH₃; R¹ is especially hydrogen.

Further particular groups of embodiments relate to the diaminotriazinecompounds of formula (I), wherein;

-   R² is H, CN, C₁-C₆-alkyl, C₁-C₆-alkoxy, (C₁-C₆-alkoxy)-C₁-C₆-alkyl,    (C₁-C₆-alkyl)carbonyl, (C₃-C₆-cycloalkyl)carbonyl,    (C₁-C₆-alkyl)sulfonyl, (C₁-C₆-alkoxy)carbonyl,    (C₁-C₆-alkylamino)carbonyl, di(C₁-C₆-alkyl)aminocarbonyl,    (C₁-C₆-alkylamino)sulfonyl, di(C₁-C₆-alkyl)aminosulfonyl, where the    aliphatic parts of the 11 aforementioned radicals are unsubstituted,    partly or completely halogenated, phenyl, phenylcarbonyl and    C₁-C₆-alkylphenyl,    -   wherein phenyl in the last 3 mentioned radical is unsubstituted        or substituted by 1, 2, 3, 4, or 5 identical or different        substituents selected from the group consisting of halogen, CN,        NO₂, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy and        C₁-C₆-haloalkoxy; preferably R² is H, CN, C₁-C₆-alkyl,        (C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkyl)carbonyl,        (C₃-C₆-cycloalkyl)carbonyl or (C₁-C₆-alkyl)sulfonyl, where the        aliphatic parts of the 4 aforementioned radicals unsubstituted        partly or completely halogenated;    -   phenyl and phenyl-C₁-C₆ alkyl,    -   wherein phenyl in the last 2 mentioned radical is unsubstituted        or substituted by 1, 2, 3, 4, or 5 identical or different        substituents selected from the group consisting of halogen, CN,        NO₂, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy and        C₁-C₆-haloalkoxy in particular R² is H, CN, C₁-C₆-alkyl,        (C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkyl)carbonyl,        (C₃-C₆-cycloalkyl)carbonyl or (C₁-C₆-alkyl)sulfonyl;    -   more particularly R² is H, CN, C₁-C₄-alkyl,        (C₁-C₄-alkoxy)-C₁-C₄-alkyl, (C₁-C₄-alkyl)carbonyl,        (C₃-C₅-cycloalkyl)carbonyl or (C₁-C₄-alkyl)sulfonyl;    -   even more particularly R² is H, CN, CH₃, CH₂CH₃, CH₂OCH₃,        C(O)CH₃, cyclopropyl-carbonyl or SO₂CH₃;    -   R² is especially hydrogen.

Further particular groups of embodiments relate to the diaminotriazinecompounds of formula (I), wherein R³ is selected from the groupconsisting of H, halogen, CN, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxyand C₁-C₆-haloalkoxy, in particular from the group consisting ofhydrogen, fluorine, chlorine C₁-C₄-alkyl such as methyl or ethyl andC₁-C₄-alkoxy, such as methoxy or ethoxy, more particularly fromhydrogen, fluorine, chlorine, methyl and methoxy, especially fromhydrogen and fluorine.

Further particular groups (1) of embodiments relate to thediaminotriazine compounds of formula (I), wherein R⁴ is selected fromthe group consisting of H, halogen, CN, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₁-C₆-alkoxy and C₁-C₆-haloalkoxy, in particular from the groupconsisting of hydrogen, fluorine and C₁-C₄-alkyl, such as methyl, ethyl,n-propyl, 2-propyl, n-butyl, 2-butyl, isobutyl or tert.-butyl,C₁-C₄-haloalkyl, such as difluoromethyl, trifluoromethyl,2,2,2-trifluoroethyl, 1,1-difluoroethyl, 1,1,2,2-tetrafluoroethyl orpentafluoroethyl, C₁-C₄-alkoxy, such as methoxy or ethoxy andC₁-C₄-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, moreparticularly from hydrogen, fluorine and methyl, especially fromhydrogen and fluorine.

In groups (1) of embodiments, R⁵ is as defined above and preferablyselected from the group consisting of C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₂-C₆-alkenyl, C₃-C₆-alkynyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl andC₁-C₆-alkoxy-C₁-C₆-alkyl, in particular from methyl, C₂-C₄-alkyl, suchas ethyl, n-propyl, 2-propyl, n-butyl, 2-butyl, isobutyl or tert.-butyl,C₁-C₄-haloalkyl, such as difluoromethyl, trifluoromethyl,2,2,2-trifluoroethyl, 1,1-difluoroethyl, 1,1,2,2-tetrafluoroethyl orpentafluoroethyl, C₂-C₄-alkenyl, such as vinyl or allyl, C₃-C₄-alkynyl,such as propargyl, C₃-C₆-cycloalkyl, such as cyclopropyl, cyclobutyl,cylopentyl or cyclohexyl, and C₁-C₄-alkoxy-C₁-C₄-alkyl, such asmethoxymethyl, ethoxymethyl, 2-methoxyethyl or 2-ethoxyethyl.

Further particular groups (2) of embodiments relate to thediaminotriazine compounds of formula (I), wherein R⁴ and R⁵ togetherwith the carbon atom to which they are attached form a moiety selectedfrom the group consisting of carbonyl, C₃-C₆-cycloalkan-1,1-diyl,ipso-C₃-C₆-cycloalkendiyl, three- to six-membered saturated or partiallyunsaturated ipso-heterocyclodiyl, where the carbocycle and theheterocycle are unsubstituted, partly or completely halogenated or carryfrom 1 to 6 C₁-C₆-alkyl groups, and the moiety >C═CR^(x)R^(y), whereR^(x) and R^(y) are hydrogen, C₁-C₄-alkyl or C₁-C₄-haloalkyl.

In groups (2) of embodiments, R⁴ and R⁵ together with the carbon atom towhich they are attached form in particular a moiety selected from thegroup consisting of C₃-C₆-cycloalkan-1,1-diyl,ipso-C₃-C₆-cycloalkendiyl, three- to six-membered saturated or partiallyunsaturated ipso-heterocyclodiyl, where the carbocycle and theheterocycle are unsubstituted, partly or completely halogenated or carryfrom 1 to 6 C₁-C₆-alkyl groups and where the heterocycle preferably has1 or 2 oxygen atoms as ring members.

In groups (2) of embodiments, R⁴ and R⁵ together with the carbon atom towhich they are attached more particularly form a moiety selected fromthe group consisting of C₃-C₆-cycloalkan-1,1-diyl or three- tosix-membered saturated ipso-heterocyclodiyl, where the carbocycle andthe heterocycle are unsubstituted, partly or completely halogenated orcarry from 1 to 6 C₁-C₆-alkyl groups, and where heterocyclyl preferablyhas 1 or 2 oxygen atoms as ring members.

Further particular groups (2a) of embodiments relate to thediaminotriazine compounds of formula (I), wherein R⁴ and R⁵ togetherwith the carbon atom to which they are attached formC₃-C₆-cycloalkan-1,1-diyl, in particular cyclopropan-1,1-diyl,cyclobutan-1,1-diyl, cyclopentan-1,1-diyl or cyclohexan-1, 1-diyl, saidC₃-C₆-cycloalkan-1,1-diyl being unsubstituted, partly or completelyhalogenated or carrying from 1 to 6 C₁-C₆-alkyl groups, in particularmethyl groups.

In groups (2a) of embodiments R⁴ and R⁵ together with the carbon atom towhich they are attached form in particular C₃-C₆-cycloalkan-1,1-diylwhich is unsubstituted. Further particular groups (2b) of embodimentsrelate to the diaminotriazine compounds of formula (I), wherein R⁴ andR⁵ together with the carbon atom to which they are attached form three-to six-membered saturated ipso-heterocyclodiyl, in particularoxiran-1,1-diyl, oxetan-1,1-diyl, oxan-1,1-diyl, oxan-1,1-diyl oroxan-4,4-diyl, said heterocycle being unsubstituted, partly orcompletely halogenated or carrying from 1 to 6 C₁-C₆-alkyl groups, inparticular groups, and where said heterocycle preferably has 1 or 2oxygen atoms as ring members. In groups (2b) of embodiments R⁴ and R⁵together with the carbon atom to which they are attached form three- tosix-membered saturated ipso-heterocyclodiyl, in particularoxiran-1,1-diyl, oxetan-1,1-diyl, oxan-1,1-diyl, oxan-1,1-diyl oroxan-4,4-diyl, said heterocycle being unsubstituted.

Particularly preferred are the diaminotriazine compounds of formula (I),and likewise the diaminotriazine compounds of formula (I) according toembodiment groups (1), (2), (2a) and (2b), wherein

-   R¹ is hydrogen;-   R² is hydrogen;-   R^(a) is selected from the group consisting of C₁-C₆-haloalkoxy,    C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy,    C₂-C₆-haloalkynyloxy, (C₁-C₆-alkoxy)-C₁-C₆-alkoxy,    C₃-C₆-cycloalkoxy, C₃-C₆-halocycloalkoxy,    (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy and    (C₃-C₆-halocycloalkyl)-C₁-C₄-alkoxy, in particular selected from the    group consisting of C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy,    C₃-C₆-cycloalkoxy, C₃-C₆-halocycloalkoxy and    (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy, more particularly from the group    consisting of C₂-C₄-alkynyloxy, such as 2-propynyloxy    (=propargyloxy), C₂-C₄-alkenyloxy, such as 2-propenyloxy    (=allyloxy), C₃-C₆-cycloalkoxy, such as cyclopropyloxy,    cyclobutyloxy, cyclopentyloxy and cyclohexyloxy, and    (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy, in particular    (C₃-C₆-cycloalkyl)-C₁-C₂-alkoxy, such as cyclopropylmethoxy,    cyclobutylmethoxy, cyclopentylmethoxy and cyclohexyl methoxy;-   R^(b) is as defined above, in particular selected from the group    consisting of halogen, such as fluorine, chlorine or bromine, CN,    C₁-C₄-alkoxy, such as methoxy or ethoxy, and C₁-C₄-haloalkoxy, such    as difluoromethoxy, trifluoromethoxy, 1,1-difluoroethoxy,    2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy and    pentafluoroethoxy, C₃-C₆-cycloalkoxy, such as cyclopropyloxy,    cyclobutyloxy, cyclopentyloxy and cyclohexyloxy and    C₃-C₆-halocycloalkoxy, more particularly from fluorine and    C₁-C₄-alkoxy, especially is fluorine; wherein in case the variable q    is 2 or 3 the two or three radicals R^(b) may be identical or    different;-   q is 0, 1, 2 or 3, in particular 0, 1 or 2.

More particularly preferred are the diaminotriazine compounds of formula(I), and likewise the diaminotriazine compounds of formula (I) accordingto embodiment groups (1), (2), (2a) and (2b), wherein

-   R¹ is hydrogen;-   R² is hydrogen;-   R^(a) is selected from the group consisting of C₂-C₆-alkenyloxy,    C₂-C₆-alkynyloxy, C₃-C₆-cycloalkoxy, C₃-C₆-halocycloalkoxy and    (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy, in particular from from    C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy, C₃-C₆-cycloalkoxy and    (C₃-C₆-cycloalkyl)-C₁-C₂-alkoxy, especially from the group    consisting of C₃-C₆-cycloalkoxy, such as cyclopropyloxy,    cyclobutyloxy, cyclopentyloxy and cyclohexyloxy, and    (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy, in particular    (C₃-C₆-cycloalkyl)-C₁-C₂-alkoxy, such as cyclopropylmethoxy,    cyclobutylmethoxy, cyclopentylmethoxy and cyclohexylmethoxy;-   R^(b) is selected from the group consisting of halogen, CN,    C₁-C₄-alkoxy and C₁-C₄-haloalkoxy, more particularly from fluorine    and C₁-C₄-alkoxy, especially is fluorine;-   q is 0, 1 or 2, in particular 0 or 1.

More particularly preferred are the diaminotriazine compounds of formula(I), and likewise the diaminotriazine compounds of formula (I) accordingto embodiment groups (1), (2), (2a) and (2b), wherein

-   R¹ is hydrogen;-   R² is hydrogen;-   R^(a) is C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy, C₃-C₆-cycloalkoxy or    (C₃-C₆-cycloalkyl)-C₁-C₂-alkoxy, in particular prop-2-enoxy,    prop-2-ynoxy, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy,    cyclohexyloxy, (cyclopropyl)methyloxy, (cyclobutyl)methyloxy,    (cyclopentyl)methyloxy or (cyclohexyl)methyloxy;-   R^(b) is fluorine, methoxy, ethoxy, n-propoxy, 2-propoxy, n-butoxy,    2-butoxy, 2-methyl-1-propoxy or tert.-butoxy, especially fluorine;-   q is 0 or 1, in particular 0.

Especially preferred are the diaminotriazine compounds of formula (I),and likewise the diaminotriazine compounds of formula (I) according toembodiment groups (1), (2), (2a) and (2b), wherein

R¹ is hydrogen;R² is hydrogen;and where the moiety of formula (A)

hereinafter moiety A—is selected from the group consisting of2-fluoro-6-(cyclopropyloxy)phenyl, 2-fluoro-6-(cyclobutyloxy)phenyl,2-fluoro-6-(cyclopentyloxy)phenyl, 2-fluoro-6-(cyclohexyloxy)phenyl,2-fluoro-6-[(cyclopropyl)methyloxy]phenyl,2-fluoro-6-[(cyclobutyl)methyloxy]phenyl,2-fluoro-6-[(cyclopentyl)methyloxy]phenyl,2-fluoro-6-[(cyclohexyl)methyloxy]phenyl, 2-fluoro-6-prop-2-enoxyphenyl,2-fluoro-6-prop-2-ynoxyphenyl, 2,3-difluoro-6-(cyclopropyloxy)phenyl,2,3-difluoro-6-(cyclobutyloxy)phenyl,2,3-difluoro-6-(cyclopentyloxy)phenyl,2,3-difluoro-6-(cyclohexyloxy)phenyl,2,3-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3-difluoro-6-prop-2-enoxyphenyl, 2,3-difluoro-6-prop-2-ynoxyphenyl,2,4-difluoro-6-(cyclopropyloxy)phenyl,2,4-difluoro-6-(cyclobutyloxy)phenyl,2,4-difluoro-6-(cyclopentyloxy)phenyl,2,4-difluoro-6-(cyclohexyloxy)phenyl,2,4-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,4-difluoro-6-prop-2-enoxyphenyl, 2,4-difluoro-6-prop-2-ynoxyphenyl,2,5-difluoro-6-(cyclopropyloxy)phenyl,2,5-difluoro-6-(cyclobutyloxy)phenyl,2,5-difluoro-6-(cyclopentyloxy)phenyl,2,5-difluoro-6-(cyclohexyloxy)phenyl,2,5-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,5-difluoro-6-prop-2-enoxyphenyl, 2,5-difluoro-6-prop-2-ynoxyphenyl,2,3,5-trifluoro-6-(cyclopropyloxy)phenyl,2,3,5-trifluoro-6-(cyclobutyloxy)phenyl,2,3,5-trifluoro-6-(cyclopentyloxy)phenyl,2,3,5-trifluoro-6-(cyclohexyloxy)phenyl,2,3,5-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,5-trifluoro-6-prop-2-enoxyphenyl,2,3,5-trifluoro-6-prop-2-ynoxyphenyl,2,4,5-trifluoro-6-(cyclopropyloxy)phenyl,2,4,5-trifluoro-6-(cyclobutyloxy)phenyl,2,4,5-trifluoro-6-(cyclopentyloxy)phenyl,2,4,5-trifluoro-6-(cyclohexyloxy)phenyl,2,4,5-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclobutyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,4,5-trifluoro-6-prop-2-enoxyphenyl,2,4,5-trifluoro-6-prop-2-ynoxyphenyl,2,3,4-trifluoro-6-(cyclopropyloxy)phenyl,2,3,4-trifluoro-6-(cyclobutyloxy)phenyl,2,3,4-trifluoro-6-(cyclopentyloxy)phenyl,2,3,4-trifluoro-6-(cyclohexyloxy)phenyl,2,3,4-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,4-trifluoro-6-prop-2-enoxyphenyl,2,3,4-trifluoro-6-prop-2-ynoxyphenyl,2,3,4,5-tretrafluoro-6-(cyclopropyloxy)phenyl,2,3,4,5-tretrafluoro-6-(cyclobutyloxy)phenyl,2,3,4,5-tretrafluoro-6-(cyclopentyloxy)phenyl,2,3,4,5-tretrafluoro-6-(cyclohexyloxy)phenyl,2,3,4,5-tretrafluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,4,5-tretrafluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3,4,5-tretrafluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,4,5-tretrafluoro-6-[(cyclohexyl)methyloxy]-phenyl,2,3,4,5-tretrafluoro-6-prop-2-enoxyphenyl and2,3,4,5-tretrafluoro-6-prop-2-ynoxyphenyl;

with preference given to 2-fluoro-6-(cyclopropyloxy)phenyl,2-fluoro-6-(cyclobutyloxy)phenyl, 2-fluoro-6-(cyclopentyloxy)phenyl,2-fluoro-6-(cyclohexyloxy)phenyl,2-fluoro-6-[(cyclopropyl)methyloxy]phenyl,2-fluoro-6-[(cyclobutyl)methyloxy]phenyl,2-fluoro-6-[(cyclopentyl)methyloxy]phenyl,2-fluoro-6-[(cyclohexyl)methyloxy]phenyl, 2-fluoro-6-prop-2-enoxyphenyl,2-fluoro-6-prop-2-ynoxyphenyl, 2,3-difluoro-6-(cyclopropyloxy)phenyl,2,3-difluoro-6-(cyclobutyloxy)phenyl,2,3-difluoro-6-(cyclopentyloxy)phenyl,2,3-difluoro-6-(cyclohexyloxy)phenyl,2,3-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3-difluoro-6-prop-2-enoxyphenyl, 2,3-difluoro-6-prop-2-ynoxyphenyl,2,4-difluoro-6-(cyclopropyloxy)phenyl,2,4-difluoro-6-(cyclobutyloxy)phenyl,2,4-difluoro-6-(cyclopentyloxy)phenyl,2,4-difluoro-6-(cyclohexyloxy)phenyl,2,4-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,4-difluoro-6-prop-2-enoxyphenyl, 2,4-difluoro-6-prop-2-ynoxyphenyl,2,5-difluoro-6-(cyclopropyloxy)phenyl,2,5-difluoro-6-(cyclobutyloxy)phenyl,2,5-difluoro-6-(cyclopentyloxy)phenyl,2,5-difluoro-6-(cyclohexyloxy)phenyl,2,5-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,5-difluoro-6-prop-2-enoxyphenyl, 2,5-difluoro-6-prop-2-ynoxyphenyl,2,3,5-trifluoro-6-(cyclopropyloxy)phenyl,2,3,5-trifluoro-6-(cyclopentyloxy)phenyl,2,3,5-trifluoro-6-(cyclohexyloxy)phenyl,2,3,5-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,4,5-trifluoro-6-(cyclopropyloxy)phenyl,2,4,5-trifluoro-6-(cyclopentyloxy)phenyl,2,4,5-trifluoro-6-(cyclohexyloxy)phenyl,2,4,5-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,4-trifluoro-6-(cyclopropyloxy)phenyl,2,3,4-trifluoro-6-(cyclopentyloxy)phenyl,2,3,4-trifluoro-6-(cyclohexyloxy)phenyl,2,3,4-trifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,4,5-tretrafluoro-6-(cyclopropyloxy)phenyl,2,3,4,5-tretrafluoro-6-(cyclopentyloxy)phenyl,2,3,4,5-tretrafluoro-6-(cyclohexyloxy)phenyl,2,3,4,5-tretrafluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,4,5-tretrafluoro-6-[(cyclopentyl)methyloxy]phenyl and2,3,4,5-tretrafluoro-6-[(cyclohexyl)methyloxy]phenyl.

Particular preference is given to diaminotriazine compounds of formula(Ia), which correspond to diaminotriazines of formula (I) wherein R¹ ishydrogen, where R², R³, R⁴ and R⁵ are as defined in the rows of thefollowing table A and wherein A is as defined in the following tablesA-1 to A-80:

In formula (I.a), the radical A corresponds to the moiety of formula(A):

where R^(a), R^(b) and q are as defined herein.

Table A-1: Compounds of the formula I.a, where A is2-fluoro-6-(cyclopropyloxy)phenyl and R², R³, R⁴ and R⁵ are as definedin rows 2 to 256 of the following table A.

Table A-2: Compounds of the formula I.a, where A is2-fluoro-6-(cyclobutyloxy)phenyl and R², R³, R⁴ and R⁵ are as defined inrows 2 to 256 of the following table A.

Table A-3: Compounds of the formula I.a, where A is2-fluoro-6-(cyclopentyloxy)phenyl and R², R³, R⁴ and R⁵ are as definedin rows 1 to 256 of the following table A.

Table A-4: Compounds of the formula I.a, where A is2-fluoro-6-(cyclohexyloxy)phenyl and R², R³, R⁴ and R⁵ are as defined inrows 1 to 256 of the following table A.

Table A-5: Compounds of the formula I.a, where A is2-fluoro-6-[(cyclopropyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-6: Compounds of the formula I.a, where A is2-fluoro-6-[(cyclobutyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-7: Compounds of the formula I.a, where A is2-fluoro-6-[(cyclopentyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-8: Compounds of the formula I.a, where A is2-fluoro-6-[(cyclohexyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-9: Compounds of the formula I.a, where A is2-fluoro-6-prop-2-enoxyphenyl and R², R³, R⁴ and R⁵ are as defined inrows 1 to 256 of the following table A.

Table A-10: Compounds of the formula I.a, where A is2-fluoro-6-prop-2-ynoxyphenyl and R², R³, R⁴ and R⁵ are as defined inrows 1 to 256 of the following table A.

Table A-11: Compounds of the formula I.a, where A is2,3-difluoro-6-(cyclopropyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-12: Compounds of the formula I.a, where A is2,3-difluoro-6-(cyclobutyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-13: Compounds of the formula I.a, where A is2,3-difluoro-6-(cyclopentyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-14: Compounds of the formula I.a, where A is2,3-difluoro-6-(cyclohexyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-15: Compounds of the formula I.a, where A is2,3-difluoro-6-[(cyclopropyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-16: Compounds of the formula I.a, where A is2,3-difluoro-6-[(cyclobutyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-17: Compounds of the formula I.a, where A is,3-difluoro-6-[(cyclopentyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-18: Compounds of the formula I.a, where A is2,3-difluoro-6-[(cyclohexyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-19: Compounds of the formula I.a, where A is2,3-difluoro-6-prop-2-enoxyphenyl and R², R³, R⁴ and R⁵ are as definedin rows 1 to 256 of the following table A.

Table A-20: Compounds of the formula I.a, where A is2,3-difluoro-6-prop-2-ynoxyphenyl and R², R³, R⁴ and R⁵ are as definedin rows 1 to 256 of the following table A.

Table A-21: Compounds of the formula I.a, where A is2,4-difluoro-6-(cyclopropyloxy)-phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-22: Compounds of the formula I.a, where A is2,4-difluoro-6-(cyclobutyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-23: Compounds of the formula I.a, where A is2,4-difluoro-6-(cyclopentyloxy)-phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-24: Compounds of the formula I.a, where A is2,4-difluoro-6-(cyclohexyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-25: Compounds of the formula I.a, where A is2,4-difluoro-6-[(cyclopropyl)-methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-26: Compounds of the formula I.a, where A is2,4-difluoro-6-[(cyclobutyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-27: Compounds of the formula I.a, where A is2,4-difluoro-6-[(cyclopentyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-28: Compounds of the formula I.a, where A is2,4-difluoro-6-[(cyclohexyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-29: Compounds of the formula I.a, where A is2,4-difluoro-6-prop-2-enoxyphenyl and R², R³, R⁴ and R⁵ are as definedin rows 1 to 256 of the following table A.

Table A-30: Compounds of the formula I.a, where A is2,4-difluoro-6-prop-2-ynoxyphenyl and R², R³, R⁴ and R⁵ are as definedin rows 1 to 256 of the following table A.

Table A-31: Compounds of the formula I.a, where A is2,5-difluoro-6-(cyclopropyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-32: Compounds of the formula I.a, where A is2,5-difluoro-6-(cyclobutyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-33: Compounds of the formula I.a, where A is2,5-difluoro-6-(cyclopentyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-34: Compounds of the formula I.a, where A is2,5-difluoro-6-(cyclohexyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-35: Compounds of the formula I.a, where A is2,5-difluoro-6-[(cyclopropyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-36: Compounds of the formula I.a, where A is2,5-difluoro-6-[(cyclobutyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-37: Compounds of the formula I.a, where A is2,5-difluoro-6-[(cyclopentyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-38: Compounds of the formula I.a, where A is2,5-difluoro-6-[(cyclohexyl)methyloxy]phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-39: Compounds of the formula I.a, where A is2,5-difluoro-6-prop-2-enoxyphenyl and R², R³, R⁴ and R⁵ are as definedin rows 1 to 256 of the following table A.

Table A-40: Compounds of the formula I.a, where A is2,5-difluoro-6-prop-2-ynoxyphenyl and R², R³, R⁴ and R⁵ are as definedin rows 1 to 256 of the following table A.

Table A-41: Compounds of the formula I.a, where A is2,3,5-trifluoro-6-(cyclopropyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-42: Compounds of the formula I.a, where A is2,3,5-trifluoro-6-(cyclobutyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-43: Compounds of the formula I.a, where A is2,3,5-trifluoro-6-(cyclopentyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-44: Compounds of the formula I.a, where A2,3,5-trifluoro-6-(cyclohexyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-45: Compounds of the formula I.a, where A is2,3,5-trifluoro-6-[(cyclopropyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-46: Compounds of the formula I.a, where A is2,3,5-trifluoro-6-[(cyclobutyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-47: Compounds of the formula I.a, where A is2,3,5-trifluoro-6-[(cyclopentyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-48: Compounds of the formula I.a, where A is2,3,5-trifluoro-6-[(cyclohexyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-49: Compounds of the formula I.a, where A is2,3,5-trifluoro-6-prop-2-enoxyphenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-50: Compounds of the formula I.a, where A is2,3,5-trifluoro-6-prop-2-ynoxyphenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-51: Compounds of the formula I.a, where A is2,4,5-trifluoro-6-(cyclopropyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-52: Compounds of the formula I.a, where A is2,4,5-trifluoro-6-(cyclobutyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-53: Compounds of the formula I.a, where A is2,4,5-trifluoro-6-(cyclopentyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-54: Compounds of the formula I.a, where A is2,4,5-trifluoro-6-(cyclohexyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-55: Compounds of the formula I.a, where A is2,4,5-trifluoro-6-[(cyclopropyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-56: Compounds of the formula I.a, where A is2,4,5-trifluoro-6-[(cyclobutyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-57: Compounds of the formula I.a, where A is2,4,5-trifluoro-6-[(cyclopentyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-58: Compounds of the formula I.a, where A is2,4,5-trifluoro-6-[(cyclohexyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-59: Compounds of the formula I.a, where A is2,4,5-trifluoro-6-prop-2-enoxyphenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-60: Compounds of the formula I.a, where A is2,4,5-trifluoro-6-prop-2-ynoxyphenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-61: Compounds of the formula I.a, where A is2,3,4-trifluoro-6-(cyclopropyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-62: Compounds of the formula I.a, where A is2,3,4-trifluoro-6-(cyclobutyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-63: Compounds of the formula I.a, where A is2,3,4-trifluoro-6-(cyclopentyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-64: Compounds of the formula I.a, where A is2,3,4-trifluoro-6-(cyclohexyloxy)phenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-65: Compounds of the formula I.a, where A is2,3,4-trifluoro-6-[(cyclopropyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-66: Compounds of the formula I.a, where A is2,3,4-trifluoro-6-[(cyclobutyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-67: Compounds of the formula I.a, where A is2,3,4-trifluoro-6-[(cyclopentyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-68: Compounds of the formula I.a, where A is2,3,4-trifluoro-6-[(cyclohexyl)methyloxy]phenyl and R², R³, R⁴ and R⁵are as defined in rows 1 to 256 of the following table A.

Table A-69: Compounds of the formula I.a, where A is2,3,4-trifluoro-6-prop-2-enoxyphenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-70: Compounds of the formula I.a, where A is2,3,4-trifluoro-6-prop-2-ynoxyphenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-71: Compounds of the formula I.a, where A is2,3,4,5-tetrafluoro-6-(cyclopropyloxy)phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-72: Compounds of the formula I.a, where A is2,3,4,5-tetrafluoro-6-(cyclobutyl-oxy)phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-73: Compounds of the formula I.a, where A is2,3,4,5-tetrafluoro-6-(cyclopentyloxy)phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-74: Compounds of the formula I.a, where A is22,3,4,5-tetrafluoro-6-(cyclohexyloxy)phenyl and R², R³, R⁴ and R⁵ areas defined in rows 1 to 256 of the following table A.

Table A-75: Compounds of the formula I.a, where A is2,3,4,5-tetrafluoro-6-[(cyclopropyl)methyloxy]phenyl and R², R³, R⁴ andR⁵ are as defined in rows 1 to 256 of the following table A.

Table A-76: Compounds of the formula I.a, where A is2,3,4,5-tetrafluoro-6-[(cyclobutyl)methyloxy]phenyl and R², R³, R⁴ andR⁵ are as defined in rows 1 to 256 of the following table A.

Table A-77: Compounds of the formula I.a, where A is2,3,4,5-tetrafluoro-6-[(cyclopentyl)methyloxy]phenyl and R², R³, R⁴ andR⁵ are as defined in rows 1 to 256 of the following table A.

Table A-78: Compounds of the formula I.a, where A is2,3,4,5-tetrafluoro-6-[(cyclohexyl)methyloxy]phenyl and R², R³, R⁴ andR⁵ are as defined in rows 1 to 256 of the following table A.

Table A-79: Compounds of the formula I.a, where A is2,3,4,5-tetrafluoro-6-prop-2-enoxyphenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

Table A-80: Compounds of the formula I.a, where A is2,3,4,5-tetrafluoro-6-prop-2-ynoxyphenyl and R², R³, R⁴ and R⁵ are asdefined in rows 1 to 256 of the following table A.

TABLE A # R² R³ R⁴ R⁵ 1 H H CH₃ CH₃ 2 H F F CH₃ 3 H F H CH₃ 4 H F CH₃CH₃ 5 H CH₃ CH₃ CH₃ 6 H F H C₂H₅ 7 H H CH₃ C₂H₅ 8 H F CH₃ C₂H₅ 9 H HOCH₃ CH₃ 10 H H OCH₃ C₂H₅ 11 H F C₂H₅ C₂H₅ 12 H H OCH₃ C₂H₅ 13 H H HCH(CH₃)₂ 14 H H F CH(CH₃)₂ 15 H F F CH(CH₃)₂ 16 H H CH₃ CH(CH₃)₂ 17 H HOCH₃ CH(CH₃)₂ 18 H F CH₃ CH(CH₃)₂ 19 H H H CH₂CH₂CH₃ 20 H H F CH₂CH₂CH₃21 H F F CH₂CH₂CH₃ 22 H H CH₃ CH₂CH₂CH₃ 23 H H OCH₃ CH₂CH₂CH₃ 24 H F CH₃CH₂CH₂CH₃ 25 H H H C(CH₃)₃ 26 H H F C(CH₃)₃ 27 H F F C(CH₃)₃ 28 H H CH₃C(CH₃)₃ 29 H H OCH₃ C(CH₃)₃ 30 H F CH₃ C(CH₃)₃ 31 H H H Cyclopropyl 32 HH F Cyclopropyl 33 H F F Cyclopropyl 34 H H CH₃ Cyclopropyl 35 H H OCH₃Cyclopropyl 36 H F CH₃ Cyclopropyl 37 H H CH₃ CF₃ 38 H F CH₃ CF₃ 39 H HCH₂—CH₂ 40 H CH₃ CH₂—CH₂ 41 H OCH₃ CH₂—CH₂ 42 H F CH₂—CH₂ 43 H ClCH₂—CH₂ 44 H H CH₂—CH₂—CH₂ 45 H CH₃ CH₂—CH₂—CH₂ 46 H OCH₃ CH₂—CH₂—CH₂ 47H F CH₂—CH₂—CH₂ 48 H Cl CH₂—CH₂—CH₂ 49 H H CH₂—CH₂—CH₂—CH₂ 50 H CH₃CH₂—CH₂—CH₂—CH₂ 51 H OCH₃ CH₂—CH₂—CH₂—CH₂ 52 H F CH₂—CH₂—CH₂—CH₂ 53 H ClCH₂—CH₂—CH₂—CH₂ 54 H H CH₂—CH₂—CH₂—CH₂—CH₂ 55 H CH₃ CH₂—CH₂—CH₂—CH₂—CH₂56 H OCH₃ CH₂—CH₂—CH₂—CH₂—CH₂ 57 H F CH₂—CH₂—CH₂—CH₂—CH₂ 58 H ClCH₂—CH₂—CH₂—CH₂—CH₂ 59 H H O—CH₂—CH₂—CH₂ 60 H CH₃ O—CH₂—CH₂—CH₂ 61 HOCF₃ O—CH₂—CH₂—CH₂ 62 H H O—CH₂—CH₂—CH₂—CH₂ 63 H CH₃ O—CH₂—CH₂—CH₂—CH₂64 H OCF₃ O—CH₂—CH₂—CH₂—CH₂ 65 CH₃ H CH₃ CH₃ 66 CH₃ F F CH₃ 67 CH₃ F HCH₃ 68 CH₃ F CH₃ CH₃ 69 CH₃ CH₃ CH₃ CH₃ 70 CH₃ F H C₂H₅ 71 CH₃ H CH₃C₂H₅ 72 CH₃ F CH₃ C₂H₅ 73 CH₃ H OCH₃ CH₃ 74 CH₃ H OCH₃ C₂H₅ 75 CH₃ FC₂H₅ C₂H₅ 76 CH₃ H OCH₃ C₂H₅ 77 CH₃ H H CH(CH₃)₂ 78 CH₃ H F CH(CH₃)₂ 79CH₃ F F CH(CH₃)₂ 80 CH₃ H CH₃ CH(CH₃)₂ 81 CH₃ H OCH₃ CH(CH₃)₂ 82 CH₃ FCH₃ CH(CH₃)₂ 83 CH₃ H H CH₂CH₂CH₃ 84 CH₃ H F CH₂CH₂CH₃ 85 CH₃ F FCH₂CH₂CH₃ 86 CH₃ H CH₃ CH₂CH₂CH₃ 87 CH₃ H OCH₃ CH₂CH₂CH₃ 88 CH₃ F CH₃CH₂CH₂CH₃ 89 CH₃ H H C(CH₃)₃ 90 CH₃ H F C(CH₃)₃ 91 CH₃ F F C(CH₃)₃ 92CH₃ H CH₃ C(CH₃)₃ 93 CH₃ H OCH₃ C(CH₃)₃ 94 CH₃ F CH₃ C(CH₃)₃ 95 CH₃ H HCyclopropyl 96 CH₃ H F Cyclopropyl 97 CH₃ F F Cyclopropyl 98 CH₃ H CH₃Cyclopropyl 99 CH₃ H OCH₃ Cyclopropyl 100 CH₃ F CH₃ Cyclopropyl 101 CH₃H CH₃ CF₃ 102 CH₃ F CH₃ CF₃ 103 CH₃ H CH₂—CH₂ 104 CH₃ CH₃ CH₂—CH₂ 105CH₃ OCH₃ CH₂—CH₂ 106 CH₃ F CH₂—CH₂ 107 CH₃ Cl CH₂—CH₂ 108 CH₃ HCH₂—CH₂—CH₂ 109 CH₃ CH₃ CH₂—CH₂—CH₂ 110 CH₃ OCH₃ CH₂—CH₂—CH₂ 111 CH₃ FCH₂—CH₂—CH₂ 112 CH₃ Cl CH₂—CH₂—CH₂ 113 CH₃ H CH₂—CH₂—CH₂—CH₂ 114 CH₃ CH₃CH₂—CH₂—CH₂—CH₂ 115 CH₃ OCH₃ CH₂—CH₂—CH₂—CH₂ 116 CH₃ F CH₂—CH₂—CH₂—CH₂117 CH₃ Cl CH₂—CH₂—CH₂—CH₂ 118 CH₃ H CH₂—CH₂—CH₂—CH₂—CH₂ 119 CH₃ CH₃CH₂—CH₂—CH₂—CH₂—CH₂ 120 CH₃ OCH₃ CH₂—CH₂—CH₂—CH₂—CH₂ 121 CH₃ FCH₂—CH₂—CH₂—CH₂—CH₂ 122 CH₃ Cl CH₂—CH₂—CH₂—CH₂—CH₂ 123 CH₃ HO—CH₂—CH₂—CH₂ 124 CH₃ CH₃ O—CH₂—CH₂—CH₂ 125 CH₃ OCF₃ O—CH₂—CH₂—CH₂ 126CH₃ H O—CH₂—CH₂—CH₂—CH₂ 127 CH₃ CH₃ O—CH₂—CH₂—CH₂—CH₂ 128 CH₃ OCF₃O—CH₂—CH₂—CH₂—CH₂ 129 CH₂CH₃ H CH₃ CH₃ 130 CH₂CH₃ F F CH₃ 131 CH₂CH₃ F HCH₃ 132 CH₂CH₃ F CH₃ CH₃ 133 CH₂CH₃ CH₃ CH₃ CH₃ 134 CH₂CH₃ F H C₂H₅ 135CH₂CH₃ H CH₃ C₂H₅ 136 CH₂CH₃ F CH₃ C₂H₅ 137 CH₂CH₃ H OCH₃ CH₃ 138 CH₂CH₃H OCH₃ C₂H₅ 139 CH₂CH₃ F C₂H₅ C₂H₅ 140 CH₂CH₃ H OCH₃ C₂H₅ 141 CH₂CH₃ H HCH(CH₃)₂ 142 CH₂CH₃ H F CH(CH₃)₂ 143 CH₂CH₃ F F CH(CH₃)₂ 144 CH₂CH₃ HCH₃ CH(CH₃)₂ 145 CH₂CH₃ H OCH₃ CH(CH₃)₂ 146 CH₂CH₃ F CH₃ CH(CH₃)₂ 147CH₂CH₃ H H CH₂CH₂CH₃ 148 CH₂CH₃ H F CH₂CH₂CH₃ 149 CH₂CH₃ F F CH₂CH₂CH₃150 CH₂CH₃ H CH₃ CH₂CH₂CH₃ 151 CH₂CH₃ H OCH₃ CH₂CH₂CH₃ 152 CH₂CH₃ F CH₃CH₂CH₂CH₃ 153 CH₂CH₃ H H C(CH₃)₃ 154 CH₂CH₃ H F C(CH₃)₃ 155 CH₂CH₃ F FC(CH₃)₃ 156 CH₂CH₃ H CH₃ C(CH₃)₃ 157 CH₂CH₃ H OCH₃ C(CH₃)₃ 158 CH₂CH₃ FCH₃ C(CH₃)₃ 159 CH₂CH₃ H H Cyclopropyl 160 CH₂CH₃ H F Cyclopropyl 161CH₂CH₃ F F Cyclopropyl 162 CH₂CH₃ H CH₃ Cyclopropyl 163 CH₂CH₃ H OCH₃Cyclopropyl 164 CH₂CH₃ F CH₃ Cyclopropyl 165 CH₂CH₃ H CH₃ CF₃ 166 CH₂CH₃F CH₃ CF₃ 167 CH₂CH₃ H CH₂—CH₂ 168 CH₂CH₃ CH₃ CH₂—CH₂ 169 CH₂CH₃ OCH₃CH₂—CH₂ 170 CH₂CH₃ F CH₂—CH₂ 171 CH₂CH₃ Cl CH₂—CH₂ 172 CH₂CH₃ HCH₂—CH₂—CH₂ 173 CH₂CH₃ CH₃ CH₂—CH₂—CH₂ 174 CH₂CH₃ OCH₃ CH₂—CH₂—CH₂ 175CH₂CH₃ F CH₂—CH₂—CH₂ 176 CH₂CH₃ Cl CH₂—CH₂—CH₂ 177 CH₂CH₃ HCH₂—CH₂—CH₂—CH₂ 178 CH₂CH₃ CH₃ CH₂—CH₂—CH₂—CH₂ 179 CH₂CH₃ OCH₃CH₂—CH₂—CH₂—CH₂ 180 CH₂CH₃ F CH₂—CH₂—CH₂—CH₂ 181 CH₂CH₃ ClCH₂—CH₂—CH₂—CH₂ 182 CH₂CH₃ H CH₂—CH₂—CH₂—CH₂—CH₂ 183 CH₂CH₃ CH₃CH₂—CH₂—CH₂—CH₂—CH₂ 184 CH₂CH₃ OCH₃ CH₂—CH₂—CH₂—CH₂—CH₂ 185 CH₂CH₃ FCH₂—CH₂—CH₂—CH₂—CH₂ 186 CH₂CH₃ Cl CH₂—CH₂—CH₂—CH₂—CH₂ 187 CH₂CH₃ HO—CH₂—CH₂—CH₂ 188 CH₂CH₃ CH₃ O—CH₂—CH₂—CH₂ 189 CH₂CH₃ OCF₃ O—CH₂—CH₂—CH₂190 CH₂CH₃ H O—CH₂—CH₂—CH₂—CH₂ 191 CH₂CH₃ CH₃ O—CH₂—CH₂—CH₂—CH₂ 192CH₂CH₃ OCF₃ O—CH₂—CH₂—CH₂—CH₂ 193 CH₂OCH₃ H CH₃ CH₃ 194 CH₂OCH₃ F F CH₃195 CH₂OCH₃ F H CH₃ 196 CH₂OCH₃ F CH₃ CH₃ 197 CH₂OCH₃ CH₃ CH₃ CH₃ 198CH₂OCH₃ F H C₂H₅ 199 CH₂OCH₃ H CH₃ C₂H₅ 200 CH₂OCH₃ F CH₃ C₂H₅ 201CH₂OCH₃ H OCH₃ CH₃ 202 CH₂OCH₃ H OCH₃ C₂H₅ 203 CH₂OCH₃ F C₂H₅ C₂H₅ 204CH₂OCH₃ H OCH₃ C₂H₅ 205 CH₂OCH₃ H H CH(CH₃)₂ 206 CH₂OCH₃ H F CH(CH₃)₂207 CH₂OCH₃ F F CH(CH₃)₂ 208 CH₂OCH₃ H CH₃ CH(CH₃)₂ 209 CH₂OCH₃ H OCH₃CH(CH₃)₂ 210 CH₂OCH₃ F CH₃ CH(CH₃)₂ 211 CH₂OCH₃ H H CH₂CH₂CH₃ 212CH₂OCH₃ H F CH₂CH₂CH₃ 213 CH₂OCH₃ F F CH₂CH₂CH₃ 214 CH₂OCH₃ H CH₃CH₂CH₂CH₃ 215 CH₂OCH₃ H OCH₃ CH₂CH₂CH₃ 216 CH₂OCH₃ F CH₃ CH₂CH₂CH₃ 217CH₂OCH₃ H H C(CH₃)₃ 218 CH₂OCH₃ H F C(CH₃)₃ 219 CH₂OCH₃ F F C(CH₃)₃ 220CH₂OCH₃ H CH₃ C(CH₃)₃ 221 CH₂OCH₃ H OCH₃ C(CH₃)₃ 222 CH₂OCH₃ F CH₃C(CH₃)₃ 223 CH₂OCH₃ H H Cyclopropyl 224 CH₂OCH₃ H F Cyclopropyl 225CH₂OCH₃ F F Cyclopropyl 226 CH₂OCH₃ H CH₃ Cyclopropyl 227 CH₂OCH₃ H OCH₃Cyclopropyl 228 CH₂OCH₃ F CH₃ Cyclopropyl 229 CH₂OCH₃ H CH₃ CF₃ 230CH₂OCH₃ F CH₃ CF₃ 231 CH₂OCH₃ H CH₂—CH₂ 232 CH₂OCH₃ CH₃ CH₂—CH₂ 233CH₂OCH₃ OCH₃ CH₂—CH₂ 234 CH₂OCH₃ F CH₂—CH₂ 235 CH₂OCH₃ Cl CH₂—CH₂ 236CH₂OCH₃ H CH₂—CH₂—CH₂ 237 CH₂OCH₃ CH₃ CH₂—CH₂—CH₂ 238 CH₂OCH₃ OCH₃CH₂—CH₂—CH₂ 239 CH₂OCH₃ F CH₂—CH₂—CH₂ 240 CH₂OCH₃ Cl CH₂—CH₂—CH₂ 241CH₂OCH₃ H CH₂—CH₂—CH₂—CH₂ 242 CH₂OCH₃ CH₃ CH₂—CH₂—CH₂—CH₂ 243 CH₂OCH₃OCH₃ CH₂—CH₂—CH₂—CH₂ 244 CH₂OCH₃ F CH₂—CH₂—CH₂—CH₂ 245 CH₂OCH₃ ClCH₂—CH₂—CH₂—CH₂ 246 CH₂OCH₃ H CH₂—CH₂—CH₂—CH₂—CH₂ 247 CH₂OCH₃ CH₃CH₂—CH₂—CH₂—CH₂—CH₂ 248 CH₂OCH₃ OCH₃ CH₂—CH₂—CH₂—CH₂—CH₂ 249 CH₂OCH₃ FCH₂—CH₂—CH₂—CH₂—CH₂ 250 CH₂OCH₃ Cl CH₂—CH₂—CH₂—CH₂—CH₂ 251 CH₂OCH₃ HO—CH₂—CH₂—CH₂ 252 CH₂OCH₃ CH₃ O—CH₂—CH₂—CH₂ 253 CH₂OCH₃ OCF₃O—CH₂—CH₂—CH₂ 254 CH₂OCH₃ H O—CH₂—CH₂—CH₂—CH₂ 255 CH₂OCH₃ CH₃O—CH₂—CH₂—CH₂—CH₂ 256 CH₂OCH₃ OCF₃ O—CH₂—CH₂—CH₂—CH₂

Especially preferred are compounds of the formula (I.b),

wherein q is 0, R¹ and R² are hydrogen and R³, R⁴ and R⁵ are defined intable A-2 below.

TABLE A-2 R^(a) R³ R⁴ R⁵ cyclopentyloxy F CH₃ CH₃ (cyclopropyl)methyloxyF CH₃ CH₃ cyclohexyloxy F CH₃ CH₃

The diaminotriazine compounds of formula (I) according to the inventioncan be prepared by standard processes of organic chemistry, for exampleby the following processes:

Process A)

The diaminotriazine compounds of formula (I), wherein R² is as definedabove and in particular H, C₁-C₆-alkyl or (C₁-C₆-alkoxy)-C₁-C₆-alkyl,can be prepared by reacting halotriazines of formula (II) with amines offormula (III) in the presence of a base and a catalyst as depicted inthe following scheme 1:

In scheme 1 and in the following schemes, the variables R¹, R² have theabove meanings while Hal is halogen, in particular bromine or chlorineand especially chlorine. In scheme 1 and in the following schemes, theradical A corresponds to the moiety of formula (A):

where R^(a), R^(b) and q are as defined herein.

Particular embodiments of the halotriazines of formula (II) relate tocompounds, where the variables Hal, R², R³, R⁴ and R⁵ have in particularthe following meanings:

-   Hal preferably Cl or Br, especially Cl;-   R² is in particular H, C₁-C₆-alkyl, (C₁-C₆-alkoxy)-C₁-C₆-alkyl;    -   more particularly H, C₁-C₄-alkoxy-C₁-C₄-alkyl, such as CH₂OCH₃;        especially hydrogen;-   R³, R⁴ and R⁵ are as defined above and in particular as defined in    embodiments (1), (2), (2a) or (2b) or in the following table B.

Particular embodiments relate to the halotriazines of formula (II.a),which correspond to the halotriazines of formula (II) wherein R² ishydrogen and Hal is Cl. Further particular embodiments relate to thehalotriazines of formula (II.b), which correspond to the halotriazinesof formula (II) wherein R² is hydrogen and Hal is Br:

Particular examples of the compounds of formulae (II.a) and (II.b) arethose, wherein R³, R⁴ and R⁵ are as defined in the following table B.

TABLE B # R³ R⁴ R⁵ 1 H CH₃ CH₃ 2 F F CH₃ 3 F H CH₃ 4 F CH₃ CH₃ 5 CH₃ CH₃CH₃ 6 F H C₂H₅ 7 H CH₃ C₂H₅ 8 F CH₃ C₂H₅ 9 H OCH₃ CH₃ 10 H OCH₃ C₂H₅ 11F C₂H₅ C₂H₅ 12 H OCH₃ C₂H₅ 13 H H CH(CH₃)₂ 14 H F CH(CH₃)₂ 15 F FCH(CH₃)₂ 16 H CH₃ CH(CH₃)₂ 17 H OCH₃ CH(CH₃)₂ 18 F CH₃ CH(CH₃)₂ 19 H HCH₂CH₂CH₃ 20 H F CH₂CH₂CH₃ 21 F F CH₂CH₂CH₃ 22 H CH₃ CH₂CH₂CH₃ 23 H OCH₃CH₂CH₂CH₃ 24 F CH₃ CH₂CH₂CH₃ 25 H H C(CH₃)₃ 26 H F C(CH₃)₃ 27 F FC(CH₃)₃ 28 H CH₃ C(CH₃)₃ 29 H OCH₃ C(CH₃)₃ 30 F CH₃ C(CH₃)₃ 31 H HCyclopropyl 32 H F Cyclopropyl 33 F F Cyclopropyl 34 H CH₃ Cyclopropyl35 H OCH₃ Cyclopropyl 36 F CH₃ Cyclopropyl 37 H CH₃ CF₃ 38 F CH₃ CF₃ 39H CH₂—CH₂ 40 CH₃ CH₂—CH₂ 41 OCH₃ CH₂—CH₂ 42 F CH₂—CH₂ 43 Cl CH₂—CH₂ 44 HCH₂—CH₂—CH₂ 45 CH₃ CH₂—CH₂—CH₂ 46 OCH₃ CH₂—CH₂—CH₂ 47 F CH₂—CH₂—CH₂ 48Cl CH₂—CH₂—CH₂ 49 H CH₂—CH₂—CH₂—CH₂ 50 CH₃ CH₂—CH₂—CH₂—CH₂ 51 OCH₃CH₂—CH₂—CH₂—CH₂ 52 F CH₂—CH₂—CH₂—CH₂ 53 Cl CH₂—CH₂—CH₂—CH₂ 54 HCH₂—CH₂—CH₂—CH₂—CH₂ 55 CH₃ CH₂—CH₂—CH₂—CH₂—CH₂ 56 OCH₃CH₂—CH₂—CH₂—CH₂—CH₂ 57 F CH₂—CH₂—CH₂—CH₂—CH₂ 58 Cl CH₂—CH₂—CH₂—CH₂—CH₂59 H O—CH₂—CH₂—CH₂ 60 CH₃ O—CH₂—CH₂—CH₂ 61 OCF₃ O—CH₂—CH₂—CH₂ 62 HO—CH₂—CH₂—CH₂—CH₂ 63 CH₃ O—CH₂—CH₂—CH₂—CH₂ 64 OCF₃ O—CH₂—CH₂—CH₂—CH₂

In formula (III)

-   R¹ is in particular H, C₁-C₆-alkyl, (C₁-C₆-alkoxy)-C₁-C₆-alkyl; more    particularly H, (C₁-C₄-alkoxy)-C₁-C₄-alkyl, such as CH₂OCH₃;    especially hydrogen; and-   A is as defined above.

The reaction of the halotriazines of formula (II) with the amines offormula (III) is usually carried out at temperatures in the range from50° C. to the boiling point of the reaction mixture, preferably from 50°C. to 150° C., particularly preferably from 60° C. to 100° C., in aninert organic solvent (e.g. P. Dao et al., Tetrahedron 2012, 68,3856-3860).

The reaction can be carried out at atmospheric pressure or underelevated pressure, if appropriate, under an inert gas, continuously orbatchwise.

In one embodiment of the process according to the invention, thehalotriazines of formula (II) and the amines of formula (III) are usedin equimolar amounts.

In another embodiment of the process according to the invention, theamines of formula (III) are used in excess with regard to thehalotriazines of formula (II).

Preferably the molar ratio of the amines of formula (III) to thehalotriazines of formula (II) is in the range from 2:1 to 1:1,preferably 1.5:1 to 1:1, especially preferred 1.2:1 to 1:1.

The reaction of the halotriazines of formula (II) with the amines offormula (III) is usually carried out in an organic solvent. Suitable inprinciple are all solvents which are capable of dissolving thehalotriazines of formula (II) and the amines of formula (II) at leastpartly and preferably fully under reaction conditions. Examples ofsuitable solvents are aliphatic hydrocarbons such as pentane, hexane,cyclohexane, nitromethane and mixtures of C₅-C₈-alkanes, aromatichydrocarbons such as benzene, chlorobenzene, toluene, cresols, o-, m-and p-xylene, halogenated hydrocarbons such as dichloromethane,1,2-dichloroethane, chloroform, carbon tetrachloride and chlorobenzene,ethers such as diethyl ether, diisopropyl ether, tert.-butyl methylether(TBME), dioxane, anisole and tetrahydrofuran (THF), esters such as ethylacetate and butyl acetate; nitriles such as acetonitrile andpropionitrile, as well as dipolar aprotic solvents such as sulfolane,dimethylsulfoxide, N,N-dimethylformamide (DMF), N,N-dimethylacetamide(DMAC), 1,3-dimethyl-2-imidazolidinone (DMI), N,N′-dimethylpropyleneurea (DMPU), dimethyl sulfoxide (DMSO) and 1-methyl-2 pyrrolidinone(NMP). Preferred solvents are ethers as defined above. The term solventas used herein also includes mixtures of two or more of the abovecompounds.

The reaction of the halotriazines of formula (II) with the amines offormula (III) is usually carried out in the presence of a base. Examplesof suitable bases include metal-containing bases and nitrogen-containingbases. Examples of suitable metal-containing bases are inorganiccompounds such as alkali metal and alkaline earth metal hydroxides, andother metal hydroxides, such as lithium hydroxide, sodium hydroxide,potassium hydroxide, magnesium hydroxide, calcium hydroxide and aluminumhydroxide; alkali metal and alkaline earth metal oxide, and other metaloxides, such as lithium oxide, sodium oxide, potassium oxide, magnesiumoxide, calcium oxide and magnesium oxide, iron oxide, silver oxide;alkali metal and alkaline earth metal hydrides such as lithium hydride,sodium hydride, potassium hydride and calcium hydride, alkali metal andalkaline earth metal formates, acetates and other metal salts ofcarboxylic acids, such as sodium formate, sodium benzoate, lithiumacetate, sodium acetate, potassium acetate, magnesium acetate, andcalcium acetate; alkali metal and alkaline earth metal carbonates suchas lithium carbonate, sodium carbonate, potassium carbonate, magnesiumcarbonate, and calcium carbonate, as well as alkali metal hydrogencarbonates (bicarbonates) such as lithium hydrogen carbonate, sodiumhydrogen carbonate, potassium hydrogen carbonate; alkali metal andalkaline earth metal phosphates such as sodium phosphate, potassiumphosphate and calcium phosphate; alkali metal and alkaline earth metalalkoxides such as sodium methoxide, sodium ethoxide, potassium ethoxide,potassium tert-butoxide, potassium tert-pentoxide anddimethoxymagnesium; and furthermore organic bases, such as tertiaryamines such as tri-C₁-C₆-alkylamines, for example triethylamine,trimethylamine, N-ethyldiisopropylamine, and N-methylpiperidine,pyridine, substituted pyridines such as collidine, lutidine,N-methylmorpholine and also bicyclic amines such as1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) or1,5-diazabicyclo[4.3.0]non-5-ene (DBN). Preferred bases are alkali metaland alkaline earth metal alkoxides as defined above. The term base asused herein also includes mixtures of two or more, preferably two of theabove compounds. Particular preference is given to the use of one base.The bases can be used in excess, preferably from 1 to 10, especiallypreferred from 2 to 4 base equivalents based on the halotriazines offormula (II), and they may also be used as the solvent.

The reaction of the halotriazines of formula (II) with the amines offormula (III) may be carried out in the presence of a catalyst. Examplesof suitable catalysts include for example, palladium based catalystslike, for example, palladium(II)acetate,tetrakis(triphenylphosphine)palladium(0),bis(triphenylphosphine)palladium(II)chloride or(1,1,-bis(diphenylphosphino)ferrocene)-dichloropalladium(II),

and optionally suitable additives such as, for example, phosphines like,for example, P(o-tolyl)₃, triphenylphosphine or BINAP(2,2′-Bis(diphenylphospino)-1,1′-binaphthyl). The amount of catalyst isusually 10 to 20 mol % (0.1 to 0.2 equivalents) based on thehalotriazines of formula (II).

The end of the reaction can easily be determined by the skilled workerby means of routine methods.

The reaction mixtures are worked up in a customary manner, for exampleby mixing with water, separation of the phases and, if appropriate,chromatographic purification of the crude product.

The amines of formula (III) used for the preparation of diaminotriazinecompounds of formula (I), wherein R¹ is H, C₁-C₆-alkyl,(C₁-C₆-alkoxy)-C₁-C₆-alkyl or C₁-C₆-alkoxy, are commercially availableand/or can be prepared by analogy to known literature.

The halotriazines of formula (II) required for the preparation ofdiaminotriazine compounds of formula (I), wherein R² is H, C₁-C₆-alkyl,(C₁-C₆-alkoxy)-C₁-C₆-alkyl or C₁-C₆-alkoxy, can be prepared by analogy(e.g. J. K. Chakrabarti et al., Tetrahedron 1975, 31, 1879-1882) byreacting thiotriazines of formula (IV) with a halogen, as depicted inscheme 2:

The variables R², R³, R⁴, R⁵ in formulae (II) and (VI) have themeanings, in particular the preferred meanings, as defined above incontext of formula (I); and the variable Hal in formula (II) has themeaning, in particular the preferred meaning, as defined above incontext of formula (II).

-   R* is C₁-C₆-alkyl, C₂-C₆-haloalkyl or phenyl;    -   in particular C₁-C₄-alkyl or C₂-C₄-haloalkyl;    -   more particularly C₁-C₄-alkyl;    -   especially CH₃.

Particular embodiments of the compounds of formula (IV) relate tocompounds, where the variables R*, R², R³, R⁴, R⁵ have in particular thefollowing meanings:

-   R* is C₁-C₆-alkyl, C₂-C₆-haloalkyl or phenyl;    -   in particular C₁-C₄-alkyl or C₂-C₄-haloalkyl;    -   more particularly C₁-C₄-alkyl;    -   especially CH₃; and-   R² is in particular H, C₁-C₆-alkyl, (C₁-C₆-alkoxy)-C₁-C₆-alkyl;    -   more particularly H, (C₁-C₄-alkoxy)-C₁-C₄-alkyl, such as        CH₂OCH₃; especially hydrogen;-   R³, R⁴ and R⁵ are as defined above and in particular as defined in    embodiments (1), (2), (2a) or (2b) or in the following table B.

Particular embodiments relate to the compounds of formula (IV.a), whichcorrespond to the compounds of formula (IV) wherein R² is hydrogen andR* is CH₃.

Particular examples of the compounds of formulae (IV.a) are those,wherein R³, R⁴ and R⁵ are as as defined in the table B above.

The reaction of the thiotriazines of formula (IV) with the halogen isusually carried out from 0° C. to the boiling point of the reactionmixture, preferably from 15° C. to the boiling point of the reactionmixture, particularly preferably from 15° C. to 40° C., in an inertorganic solvent (e.g. J. K.

Chakrabarti et al., Tetrahedron 1975, 31, 1879-1882).

The reaction can be carried out at atmospheric pressure or underelevated pressure, if appropriate under an inert gas, continuously orbatchwise.

In the reaction of the thiotriazines of formula (IV) with halogen, thehalogen is generally used in excess with regard to the thiotriazine offormula (IV).

The reaction of the thiotriazines of formula (IV) with halogen isusually carried out in an organic solvent.

Suitable in principle are all solvents which are capable of dissolvingthe thiotriazines of formula (IV) and the halogen at least partly andpreferably fully under reaction conditions.

Examples of suitable solvents are aliphatic hydrocarbons such aspentane, hexane, cyclohexane and mixtures of C₅-C₈-alkanes, halogenatedhydrocarbons such as dichloromethane, 1,2-dichloroethane, chloroform andcarbon tetrachloride; ethers such as diethyl ether, diisopropyl ether,tert.-butyl methylether (TBME), dioxane, anisole and tetrahydrofuran(THF), alcohols such as methanol, ethanol, n-propanol, isopropanol,n-butanol and tert.-butanol, as well as organic acids like formic acid,acetic acid, propionic acid, oxalic acid, citric acid, trifluoroaceticacid. Preferred solvents are halogenated hydrocarbons and organic acidsas defined above. The term solvent as used herein also includes mixturesof two or more of the above compounds. The end of the reaction caneasily be determined by the skilled worker by means of routine methods.The reaction mixtures are worked up in a customary manner, for exampleby mixing with water, separation of the phases and, if appropriate,chromatographic purification of the crude product.

The halotriazines of formula (II) required for the preparation ofdiaminotriazine compounds of formula (I), wherein R² is H, C₁-C₆-alkylor (C₁-C₆-alkoxy)-C₁-C₆-alkyl, can also be prepared by reacting2,4-dichlorotriazines of formula (VII) with a an amine H₂N—R², inparticular with ammonia, as depicted in scheme 3: Scheme 3:

The variables R², R³, R⁴, R⁵ in formulae (II) and (VII) have themeanings, in particular the preferred meanings, as defined above incontext of formula (I).

Hal and Hal′ are each, independently, halogen, in particular bromine orchlorine, especially chlorine.

The reaction depicted in scheme 3 can be performed by simply mixing therequired amounts of the compound of formula (VII) with the amine H₂N—R²or by analogy to the reaction depicted in scheme 1.

Preferably the molar ratio of the amine to the halotriazines of formula(II) is in the range from 10:1 to 1:1, preferably 5:1 to 1:1.

The reaction depicted in scheme 3 is preferably carried out in an inertsolvent. Examples of suitable solvents are nitromethane, aromatichydrocarbons such as benzene, chlorobenzene, toluene, cresols, o-, m-and p-xylene, halogenated hydrocarbons such as dichloromethane,1,2-dichloroethane, chloroform, carbon tetrachloride and chlorobenzene,ethers such as diethyl ether, diisopropyl ether, tert.-butyl methylether(TBME), dioxane, anisole and tetrahydrofuran (THF), esters such as ethylacetate and butyl acetate; nitriles such as acetonitrile andpropionitrile, as well as dipolar aprotic solvents such as sulfolane,dimethylsulfoxide, N,N-dimethylformamide (DMF), N,N-dimethylacetamide(DMAC), 1,3-dimethyl-2-imidazolidinone (DMI), N,N′-dimethylpropyleneurea (DMPU), dimethyl sulfoxide (DMSO) and 1-methyl-2 pyrrolidinone(NMP) and mixtures thereof with with water or with aliphatichydrocarbons such as pentane, hexane, cyclohexane or with mixtures ofC₅-C₈-alkane. Preferred solvents are ethers as defined above andmixtures thereof with water. The term solvent as used herein alsoincludes mixtures of two or more of the above compounds.

The reaction depicted in scheme 3 may be performed in the presence of anauxiliary base. Suitable bases are those mentioned in context with thereaction depicted in scheme 1.

However, the amine H₂N—R² may itself serve as an auxiliary base. In thiscase, usually an excess of the amine H₂N—R² is used.

Process B)

The diaminotriazine compounds of formula (I), wherein

-   R² is different from hydrogen, e.g. C₁-C₆-alkyl,    (C₁-C₆-alkoxy)-C₁-C₆-alkyl, CN, (C₁-C₆-alkyl)carbonyl,    (C₁-C₆-alkoxy)carbonyl, (C₁-C₆-alkyl)sulfonyl, phenylsulfonyl,    phenyl, phenyl-C₁-C₆ alkyl, phenylcarbonyl or phenoxycarbonyl,    -   wherein the phenyl is unsubstituted or substituted as defined        above for the respective radicals in formula (I),    -   can be prepared by reacting azines of formula (I), wherein R² is        hydrogen with a compound of formula (V) as depicted in scheme 4:

The variables A, R¹, R², R³, R⁴, R⁵ have the meanings, in particular thepreferred meanings, as in formula (I) mentioned above,

-   R² is different from hydrogen, e.g. C₁-C₆-alkyl,    (C₁-C₆-alkoxy)-C₁-C₆-alkyl, CN, (C₁-C₆-alkyl)carbonyl,    (C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl,    (C₁-C₆-alkyl)sulfonyl, phenylsulfonyl, phenyl, phenyl-C₁-C₆ alkyl,    phenylcarbonyl or phenoxycarbonyl, wherein the phenyl is    unsubstituted or substituted as defined above for the respective    radicals in formula (I);    -   in particular C₁-C₄-alkyl, CN, (C₁-C₆-alkyl)carbonyl,        (C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl or        (C₁-C₆-alkyl)sulfonyl;    -   especially CN, COCH₃, cyclopropyl-carbonyl, COOCH₃ or SO₂CH₃;        and-   Y is halogen or oxycarbonyl-C₁-C₆-alkyl;    -   in particular halogen;    -   especially Cl, I or Br.

Process C)

The diaminotriazine compounds of formula (I), wherein

-   R¹ is is different from hydrogen, e.g. C₁-C₆-alkyl,    (C₁-C₆-alkoxy)-C₁-C₆-alkyl, CN, (C₁-C₆-alkyl)carbonyl,    (C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl,    (C₁-C₆-alkyl)sulfonyl, phenylsulfonyl, phenyl, phenyl-C₁-C₆ alkyl,    phenylcarbonyl or phenoxycarbonyl, wherein the phenyl is    unsubstituted or substituted by one to five substituents selected    from the group consisting of halogen, CN, NO₂, C₁-C₆-alkyl,    C₁-C₆-haloalkyl and C₁-C₆-alkoxy,    -   can be prepared by reacting azines of formula (I), wherein R¹ is        hydrogen with a compound of formula (VI), as depectied in scheme        5:

The variables A, R¹, R², R³, R⁴, R⁵ have the meanings, in particular thepreferred meanings, as in formula (I) mentioned above,

-   R¹ is different from hydrogen, e.g. C₁-C₆-alkyl,    (C₁-C₆-alkoxy)-C₁-C₆-alkyl, CN, (C₁-C₆-alkyl)carbonyl,    (C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl,    (C₁-C₆-alkyl)sulfonyl, phenylsulfonyl, phenyl, phenyl-C₁-C₆ alkyl,    phenylcarbonyl or phenoxycarbonyl, wherein the phenyl is    unsubstituted or substituted as defined above for the respective    radicals in formula (I);    -   in particular C₁-C₄-alkyl, CN, (C₁-C₆-alkyl)carbonyl,        (C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl or        (C₁-C₆-alkyl)sulfonyl;    -   especially CN, COCH₃, cyclopropyl-carbonyl, COOCH₃ or SO₂CH₃;        and-   Z is halogen or oxycarbonyl-C₁-C₆-alkyl;    -   in particular halogen;    -   especially Cl, I or Br.

Both processes B and C independently of one another are usually carriedout at from 0° C. to the boiling point of the reaction mixture,preferably from 23° C. to 130° C., particularly preferably from 23° C.to 100° C., (e.g. Y. Yuki et al., Polym. J. 1992, 24, 791-799).

Both processes B and C independently of one another can be carried outat atmospheric pressure or under elevated pressure, if appropriate underan inert gas, continuously or batchwise.

In one embodiment of processes B and C according to the inventionindependently of one another, the diaminotriazine compounds of formula(I), wherein R², or R¹ respectively, is hydrogen are used in excess withregard to the compound of formula (V), or (VI) respectively.

In another embodiment of processes B and C according to the inventionindependently of one another, the diaminotriazine compounds of formula(I), wherein R², or R¹ respectively, is hydrogen and the compound offormula (V), or (VI) respectively, are used in equimolar amounts.

Preferably the molar ratio of the diaminotriazine compounds of formula(I), wherein R², or R¹ respectively, is hydrogen to the compound offormula (V), or (VI) respectively, is in the range from 1:1.5 to 1:1,preferably 1:1.2 to 1:1, especially preferred 1:1.

Both processes B and C independently of one another are usually carriedout in an organic solvent. Suitable in principle are all solvents whichare capable of dissolving the diaminotriazine compounds of formula (I),wherein R², or R¹ respectively, is hydrogen and the compound of formula(V), or (VI) respectively, at least partly and preferably fully underreaction conditions. Examples of suitable solvents are halogenatedhydrocarbons such as dichloromethane, 1,2-dichloroethane, chloroform,carbon tetrachloride and chlorobenzene; ethers such as diethyl ether,diisopropyl ether, tert.-butyl methylether (TBME), dioxane, anisole andtetrahydrofuran (THF); nitriles such as acetonitrile and propionitrile;alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanoland tert.-butanol; organic acids like formic acid, acetic acid,propionic acid, oxalic acid, methylbenzenesulfonic acid, benzenesulfonicacid, camphorsulfonic acid, citric acid, trifluoroacetic acid as well asdipolar aprotic solvents such as sulfolane, dimethylsulfoxide,N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMAC),1,3-dimethyl-2-imidazolidinone (DMI), N,N′-dimethylpropylene urea(DMPU), dimethyl sulfoxide (DMSO) and 1-methyl-2 pyrrolidinone (NMP).Preferred solvents are halogenated hydrocarbons, ethers and dipolaraprotic solvents as mentioned above. More preferred solvents aredichloromethane or dioxane. It is also possible to use mixtures of thesolvents mentioned. The term solvent as used herein also includesmixtures of two or more of the above compounds.

Both processes B and C independently of one another are optionallycarried out in the presence of a base. Examples of suitable basesinclude metal-containing bases and nitrogen-containing bases. Examplesof suitable metal-containing bases are inorganic compounds such asalkali metal and alkaline earth metal hydrides such as lithium hydride,sodium hydride, potassium hydride and calcium hydride, alkali metal andalkaline earth metal carbonates such as lithium carbonate, sodiumcarbonate, potassium carbonate, magnesium carbonate, and calciumcarbonate, as well as alkali metal hydrogen carbonates (bicarbonates)such as lithium hydrogen carbonate, sodium hydrogen carbonate, potassiumhydrogen carbonate; alkali metal and alkaline earth metal phosphatessuch as sodium phosphate, potassium phosphate and calcium phosphate; andfurthermore organic bases, such as tertiary amines such astri-C₁-C₆-alkylamines, for example triethylamine, trimethylamine,N-ethyldiisopropylamine, and N-methylpiperidine, pyridine, substitutedpyridines such as collidine, lutidine, N-methylmorpholine and4-dimethylaminopyridine (DMAP), and also bicyclic amines such as1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) or1,5-diazabicyclo[4.3.0]non-5-ene (DBN). Preferred bases are organicbases and alkali metal carbonates as mentioned above. Especiallypreferred bases are organic bases as mentioned above. The term base asused herein also includes mixtures of two or more, preferably two of theabove compounds. The bases are generally employed in excess; howeverthey can also be employed in equimolar amounts, or, if appropriate, canbe used as solvent. Preferably from 1 to 5 base equivalents,particularly preferred 3 base equivalents of base are used, based on thediaminotriazine compounds of formula (I).

Work-up of the reaction mixture is performed by standard procedures.

The compounds of formula (V), or (VI) respectively, are known compounds.They are commercially available or can be prepared in analogy to knownmethods.

Process D)

The diaminotriazine compounds of formula (I), wherein R¹ and R² are asdefined above, can be prepared by reacting biguanidines of formula (VII)with carbonyl compounds of formula (VIII) in the presence of a base:

The variables A, R¹, R², R³, R⁴, R⁵ have the meanings, in particular thepreferred meanings, as in formula (I) mentioned above, while

-   L¹ is a nucleophilically displaceable leaving group such as halogen,    CN, C₁-C₆-alkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-alkylcarbonyloxy or    C₁-C₆-alkoxycarbonyloxy; preferably halogen or C₁-C₆-alkoxy;

particularly preferred Cl or C₁-C₆-alkoxy,

also particularly preferred halogen;

especially preferred Cl.

The reaction of biguanidines of formula (VII) with carbonyl compounds offormula (VIII) is usually carried out at temperatures from 50° C. to theboiling point of the reaction mixture, preferably from 50° C. to 200° C.(e.g. R. Sathunuru et al., J. Heterocycl. Chem. 2008, 45, 1673-1678).

The reaction can be carried out at atmospheric pressure or underelevated pressure, if appropriate under an inert gas, continuously orbatchwise.

In one embodiment of the process according to the invention, thebiguanidines of formula (VII) and the carbonyl compounds of formula(VIII) are used in equimolar amounts.

In another embodiment of the process according to the invention, thecarbonyl compounds of formula (VIII) are used in excess with regard tothe biguanidines of formula (VII).

Preferably the molar ratio of the carbonyl compounds of formula (VIII)to the biguanidines of formula (VII) is in the range from 1.5:1 to 1:1,preferably 1.2:1 to 1:1, especially preferred 1.2:1 to 1:1, alsoespecially preferred 1:1.

The reaction of the biguanidines of formula (VII) with the carbonylcompounds of formula (VIII) is carried out in an organic solvent.

Suitable in principle are all solvents which are capable of dissolvingthe biguanidines of formula (VII) and the carbonyl compounds of formula(VIII) at least partly and preferably fully under reaction conditions.

Examples of suitable solvents are

aliphatic hydrocarbons such as pentane, hexane, cyclohexane,nitromethane and mixtures of C₅-C₈-alkanes; romatic hydrocarbons such asbenzene, chlorobenzene, toluene, cresols, o-, m- and p-xylene;halogenated hydrocarbons such as dichloromethane, 1,2-dichloroethane,chloroform, carbon tetrachloride and chlorobenzene, ethers such asdiethyl ether, diisopropyl ether, tert.-butyl methylether (TBME),dioxane, anisole and tetrahydrofuran (THF), nitriles such asacetonitrile and propionitrile, as well as dipolar aprotic solvents suchas sulfolane, dimethylsulfoxide, N,N-dimethylformamide (DMF),N,N-dimethylacetamide (DMAC), 1,3-dimethyl-2-imidazolidinone (DMI),N,N′-dimethylpropylene urea (DMPU), dimethyl sulfoxide (DMSO) and1-methyl-2 pyrrolidinone (NMP).

Preferred solvents are ethers and dipolar aprotic solvents as definedabove.

More preferred solvents are ethers as defined above.

The term solvent as used herein also includes mixtures of two or more ofthe above compounds.

The reaction of the biguanidines of formula (VII) with the carbonylcompounds of formula (VIII) is carried out in the presence of a base.

Examples of suitable bases include metal-containing bases andnitrogen-containing bases.

Examples of suitable metal-containing bases are inorganic compounds suchas alkali metal and alkaline earth metal oxide, and other metal oxides,such as lithium oxide, sodium oxide, potassium oxide, magnesium oxide,calcium oxide and magnesium oxide, iron oxide, silver oxide; alkalimetal and alkaline earth metal hydrides such as lithium hydride, sodiumhydride, potassium hydride and calcium hydride, alkali metal amides suchas lithium amide, sodium amide and potassium amide, alkali metal andalkaline earth metal carbonates such as lithium carbonate, sodiumcarbonate, potassium carbonate, magnesium carbonate, and calciumcarbonate, as well as alkali metal hydrogen carbonates (bicarbonates)such as lithium hydrogen carbonate, sodium hydrogen carbonate, potassiumhydrogen carbonate; alkali metal and alkaline earth metal phosphatessuch as sodium phosphate, potassium phosphate and calcium phosphate; andfurthermore organic bases, such as tertiary amines such astri-C₁-C₆-alkylamines, for example triethylamine, trimethylamine,N-ethyldiisopropylamine, and N-methylpiperidine, pyridine, substitutedpyridines such as collidine, lutidine, N-methylmorpholine and4-dimethylaminopyridine (DMAP), and also bicyclic amines such as1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) or1,5-diazabicyclo[4.3.0]non-5-ene (DBN).

Preferred bases are tri-C₁-C₆-alkylamines as defined above.

The term base as used herein also includes mixtures of two or more,preferably two of the above compounds. Particular preference is given tothe use of one base.

The bases are generally employed in excess; however they can also beemployed in equimolar amounts, or, if appropriate, can be used assolvent.

Preferably from 1 to 5 base equivalents, particularly preferred 3 baseequivalents of base are used, based on the biguanidines of formula(VII).

The end of the reaction can easily be determined by the skilled workerby means of routine methods.

The reaction mixtures are worked up in a customary manner, for exampleby mixing with water, separation of the phases and, if appropriate,chromatographic purification of the crude product.

Some of the intermediates and end products are obtained in the form ofviscous oils, which can be purified or freed from volatile componentsunder reduced pressure and at moderately elevated temperature.

If the intermediates and the end products are obtained as solids,purification can also be carried out by recrystallisation or digestion.

The carbonyl compounds of formula (VIII) required for the preparation ofazines of formula (I) are known in the art and can be be prepared inanalogy of known methods and/or are commercially available.

The biguanidines of formula (VII) required for the preparation of azinesof formula (I), wherein R¹ and R² are defined above, can be prepared byreacting guanidines of formula (IX) with amines of formula (X) in thepresence of an acid:

The variable A has the meanings, in particular the preferred meanings,as in formula (I) mentioned above.

The reaction of guanidines of formula (IX) with amines of formula (X) isusually carried out from 50° C. to 150° C., preferably from 80° C. to130° C.

Microwave technology was used where applicable (e.g. C. O. Kappe, A.Stadler, Microwaves in Organic and Medicinal Chemistry, Weinheim 2012).

The reaction can be carried out at atmospheric pressure or underelevated pressure, if appropriate under an inert gas, continuously orbatchwise.

In one embodiment of the process according to the invention, theguanidines of formula (IX) and the amines of formula (X) are used inequimolar amounts.

In another embodiment of the process according to the invention, theamines of formula (X) are used in excess with regard to the guanidinesof formula (IX).

Preferably the molar ratio of the amines of formula (X) to theguanidines of formula (IX) is in the range from 2:1 to 1:1, preferably1.5:1 to 1:1, especially preferred 1:1.

The reaction of the guanidines of formula (IX) with the amines offormula (X) is carried out in an organic solvent.

Suitable in principle are all solvents which are capable of dissolvingthe guanidines of formula (IX) and the amines of formula (X) at leastpartly and preferably fully under reaction conditions.

Examples of suitable solvents are aliphatic hydrocarbons such aspentane, hexane, cyclohexane, nitromethane and mixtures ofC₅-C₈-alkanes, aromatic hydrocarbons such as benzene, chlorobenzene,toluene, cresols, o-, m- and p-xylene, halogenated hydrocarbons such asdichloromethane, 1,2-dichloroethane, chloroform, carbon tetrachlorideand chlorobenzene, ethers such as diethyl ether, diisopropyl ether,tert.-butyl methylether (TBME), dioxane, anisole and tetrahydrofuran(THF), esters such as ethyl acetate and butyl acetate, nitriles such asacetonitrile and propionitrile, as well as dipolar aprotic solvents suchas sulfolane, dimethylsulfoxide, N,N-dimethylformamide (DMF),N,N-dimethylacetamide (DMAC), 1,3-dimethyl-2-imidazolidinone (DMI),N,N′-dimethylpropylene urea (DMPU), dimethyl sulfoxide (DMSO) and1-methyl-2 pyrrolidinone (NMP).

Preferred solvents are ethers, nitriles and dipolar aprotic solvents asdefined above.

More preferred solvents are nitriles as defined above.

The term solvent as used herein also includes mixtures of two or more ofthe above compounds.

The reaction of the guanidines of formula (IX) with the amines offormula (X) is carried out in the presence of an acid.

As acids and acidic catalysts inorganic acids like hydrofluoric acid,hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid,sulfuric acid; mineral acids like hydrochloric acid, sulfuric acid,phosphoric acid, Lewis acids like boron trifluoride, aluminium chloride,ferric-Ill-chloride, tin-IV-chloride, titanium-IV-chloride andzinc-II-chloride, as well as organic acids like formic acid, aceticacid, propionic acid, oxalic acid, methylbenzenesulfonic acid,benzenesulfonic acid, camphorsulfonic acid, citric acid, trifluoroaceticacid, can be used.

The acids are generally employed in excess or, if appropriate, can beused as solvent.

Work up can be carried out in a known manner.

The guanidines of formula (IX) required for the preparation ofbiguanidines of formula (VII) are commercially available or can beprepared in accordance with literature procedures (e.g. J. L. LaMattinaet al., J. Med. Chem. 1990, 33, 543-552; A. Perez-Medrano et al., J.Med. Chem. 2009, 52, 3366-3376).

The amines of formula (X) required for the preparation of biguanidinesof formula (VII) are commercially available.

The compounds of formula (I) have herbicidal activity. Therefore, theycan be used for controlling unwanted or undesired plants or vegetation.They can also be used in a method for controlling unwanted or undesiredplants or vegetation, which method comprises allowing at least onecompound of formula (I) or a salt thereof to act on plants, theirenvironment or on seed. In order to allow the compound of formula (I) ora salt thereof to act on plants, their environment or on seed thecompounds of the invention are applied to the plants, their environmentor to the seed of said plants.

To widen the spectrum of action and to achieve synergistic effects, thediaminotriazine compounds of formula (I) may be mixed with a largenumber of representatives of other herbicidal or growth-regulatingactive ingredient groups and then applied concomitantly.

Suitable components for mixtures are, for example, herbicides from theclasses of the acetamides, amides, aryloxyphenoxypropionates,benzamides, benzofuran, benzoic acids, benzothiadiazinones,bipyridylium, carbamates, chloroacetamides, chlorocarboxylic acids,cyclohexanediones, dinitroanilines, dinitrophenol, diphenyl ether,glycines, imidazolinones, isoxazoles, isoxazolidinones, nitriles,N-phenylphthalimides, oxadiazoles, oxazolidinediones, oxyacetamides,phenoxycarboxylic acids, phenylcarbamates, phenylpyrazoles,phenylpyrazolines, phenylpyridazines, phosphinic acids,phosphoroamidates, phosphorodithioates, phthalamates, pyrazoles,pyridazinones, pyridines, pyridinecarboxylic acids,pyridinecarboxamides, pyrimidinediones, pyrimidinyl(thio)benzoates,quinolinecarboxylic acids, semicarbazones,sulfonylaminocarbonyltriazolinones, sulfonylureas, tetrazolinones,thiadiazoles, thiocarbamates, triazines, triazinones, triazoles,triazolinones, triazolocarboxamides, triazolopyrimidines, triketones,uracils, ureas.

The invention also relates to combinations of diaminotriazine compoundsof formula (I) with at least one further herbicide B and/or at least onesafener C).

The further herbicidal compound B (component B) is in particularselected from the herbicides of class b1) to b15):

-   -   b1) lipid biosynthesis inhibitors;    -   b2) acetolactate synthase inhibitors (ALS inhibitors);    -   b3) photosynthesis inhibitors;    -   b4) protoporphyrinogen-IX oxidase inhibitors,    -   b5) bleacher herbicides;    -   b6) enolpyruvyl shikimate 3-phosphate synthase inhibitors (EPSP        inhibitors);    -   b7) glutamine synthetase inhibitors;    -   b8) 7,8-dihydropteroate synthase inhibitors (DHP inhibitors);    -   b9) mitosis inhibitors;    -   b10) inhibitors of the synthesis of very long chain fatty acids        (VLCFA inhibitors);    -   b11) cellulose biosynthesis inhibitors;    -   b12) decoupler herbicides;    -   b13) auxinic herbicides;    -   b14) auxin transport inhibitors; and    -   b15) other herbicides selected from the group consisting of        bromobutide, chlorflurenol, chlorflurenol-methyl, cinmethylin,        cumyluron, dalapon, dazomet, difenzoquat,        difenzoquat-metilsulfate, dimethipin, DSMA, dymron, endothal and        its salts, etobenzanid, flamprop, flamprop-isopropyl,        flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl,        flurenol, flurenol-butyl, flurprimidol, fosamine,        fosamine-ammonium, indanofan, indaziflam, maleic hydrazide,        mefluidide, metam, methiozolin (CAS 403640-27-7), methyl azide,        methyl bromide, methyl-dymron, methyl iodide, MSMA, oleic acid,        oxaziclomefone, pelargonic acid, pyributicarb, quinoclamine,        triaziflam, tridiphane and        6-chloro-3-(2-cyclopropyl-6-methylphenoxy)-4-pyridazinol (CAS        499223-49-3) and its salts and esters;

;

including their agriculturally acceptable salts or derivatives such asethers, esters or amides.

In one embodiment of the present invention the compositions according tothe present invention comprise at least one diaminotriazine compound offormula (I) and at least one further active compound B (herbicide B).

According to a further embodiment of the invention the compositionscontain at least one inhibitor of the lipid biosynthesis (herbicide b1).These are compounds that inhibit lipid biosynthesis. Inhibition of thelipid biosynthesis can be affected either through inhibition ofacetylCoA carboxylase (hereinafter termed ACC herbicides) or through adifferent mode of action (hereinafter termed non-ACC herbicides). TheACC herbicides belong to the group A of the HRAC classification systemwhereas the non-ACC herbicides belong to the group N of the HRACclassification.

According to a further embodiment of the invention the compositionscontain at least one ALS inhibitor (herbicide b2). The herbicidalactivity of these compounds is based on the inhibition of acetolactatesynthase and thus on the inhibition of the branched chain amino acidbiosynthesis. These inhibitors belong to the group B of the HRACclassification system.

According to a further embodiment of the invention the compositionscontain at least one inhibitor of photosynthesis (herbicide b3). Theherbicidal activity of these compounds is based either on the inhibitionof the photosystem II in plants (so-called PSII inhibitors, groups C1,C2 and C3 of HRAC classification) or on diverting the electron transferin photosystem I in plants (so-called PSI inhibitors, group D of HRACclassification) and thus on an inhibition of photosynthesis. Amongstthese, PSII inhibitors are preferred.

According to a further embodiment of the invention the compositionscontain at least one inhibitor of protoporphyrinogen-IX-oxidase(herbicide b4). The herbicidal activity of these compounds is based onthe inhibition of the protoporphyrinogen-IX-oxidase. These inhibitorsbelong to the group E of the HRAC classification system.

According to a further embodiment of the invention the compositionscontain at least one bleacher-herbicide (herbicide b5). The herbicidalactivity of these compounds is based on the inhibition of the carotenoidbiosynthesis. These include compounds which inhibit carotenoidbiosynthesis by inhibition of phytoene desaturase (so-called PDSinhibitors, group F1 of HRAC classification), compounds that inhibit the4-hydroxyphenyl-pyruvate-dioxygenase (HPPD inhibitors, group F2 of HRACclassification), compounds that inhibit DOXsynthase (group F4 of HRACclass) and compounds which inhibit carotenoid biosynthesis by an unknownmode of action (bleacher—unknown target, group F3 of HRACclassification).

According to a further embodiment of the invention the compositionscontain at least one EPSP synthase inhibitor (herbicide b6). Theherbicidal activity of these compounds is based on the inhibition ofenolpyruvyl shikimate 3-phosphate synthase, and thus on the inhibitionof the amino acid biosynthesis in plants. These inhibitors belong to thegroup G of the HRAC classification system.

According to a further embodiment of the invention the compositionscontain at least one glutamine synthetase inhibitor (herbicide b7). Theherbicidal activity of these compounds is based on the inhibition ofglutamine synthetase, and thus on the inhibition of the aminoacidbiosynthesis in plants. These inhibitors belong to the group H of theHRAC classification system.

According to an further embodiment of the invention the compositionscontain at least one DHP synthase inhibitor (herbicide b8). Theherbicidal activity of these compounds is based on the inhibition of7,8-dihydropteroate synthase. These inhibitors belong to the group I ofthe HRAC classification system.

According to a further embodiment of the invention the compositionscontain at least one mitosis inhibitor (herbicide b9). The herbicidalactivity of these compounds is based on the disturbance or inhibition ofmicrotubule formation or organization, and thus on the inhibition ofmitosis. These inhibitors belong to the groups K1 and K2 of the HRACclassification system. Among these, compounds of the group K1, inparticular dinitroanilines, are preferred.

According to a further embodiment of the invention the compositionscontain at least one VLCFA inhibitor (herbicide b10). The herbicidalactivity of these compounds is based on the inhibition of the synthesisof very long chain fatty acids and thus on the disturbance or inhibitionof cell division in plants. These inhibitors belong to the group K3 ofthe HRAC classification system.

According to an further embodiment of the invention the compositionscontain at least one cellulose biosynthesis inhibitor (herbicide b11).The herbicidal activity of these compounds is based on the inhibition ofthe biosynthesis of cellulose and thus on the inhibition of thesynthesis of cell walls in plants. These inhibitors belong to the groupL of the HRAC classification system.

According to a further embodiment of the invention the compositionscontain at least one decoupler herbicide (herbicide b12). The herbicidalactivity of these compounds is based on the disruption of the cellmembrane. These inhibitors belong to the group M of the HRACclassification system.

According to a further embodiment of the invention the compositionscontain at least one auxinic herbicide (herbicide b13). These includecompounds that mimic auxins, i.e. plant hormones, and affect the growthof the plants. These compounds belong to the group O of the HRACclassification system.

According to a further embodiment of the invention the compositionscontain at least one auxin transport inhibitor (herbicide b14). Theherbicidal activity of these compounds is based on the inhibition of theauxin transport in plants. These compounds belong to the group P of theHRAC classification system.

As to the given mechanisms of action and classification of the activesubstances, see e.g. “HRAC, Classification of Herbicides According toMode of Action”, http://www.plantprotection.org/hrac/MOA.html).

Preference is given to those compositions according to the presentinvention comprising at least one herbicide B selected from herbicidesof class b1, b6, b9, b10 and b11.

Preference is also given to those compositions according to the presentinvention comprising at least one herbicide B selected from herbicidesof class b2, b3, b4, b5, b6, b9 and b10.

Specific preference is given to those compositions according to thepresent invention which comprise at least one herbicide B selected fromthe herbicides of class b4, b6 b9 and b10.

Particular preference is given to those compositions according to thepresent invention which comprise at least one herbicide B selected fromthe herbicides of class b4, b6 and b10.

Examples of herbicides B which can be used in combination with thediaminitriazine compounds of formula (I) according to the presentinvention are:

b1) from the group of the lipid biosynthesis inhibitors:

ACC-herbicides such as alloxydim, alloxydim-sodium, butroxydim,clethodim, clodinafop, clodinafop-propargyl, cycloxydim, cyhalofop,cyhalofop-butyl, diclofop, diclofop-methyl, fenoxaprop,fenoxaprop-ethyl, fenoxaprop-P, fenoxaprop-P-ethyl, fluazifop,fluazifop-butyl, fluazifop-P, fluazifop-P-butyl, haloxyfop,haloxyfop-methyl, haloxyfop-P, haloxyfop-P-methyl, metamifop, pinoxaden,profoxydim, propaquizafop, quizalofop, quizalofop-ethyl,quizalofop-tefuryl, quizalofop-P, quizalofop-P-ethyl,quizalofop-P-tefuryl, sethoxydim, tepraloxydim, tralkoxydim,

4-(4′-Chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one (CAS1312337-72-6);4-(2′,4′-Dichloro-4-cyclopropyl[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1312337-45-3);4-(4′-Chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1033757-93-5);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-2,2,6,6-tetramethyl-2H-pyran-3,5(4H,6H)-dione(CAS 1312340-84-3);5-(Acetyloxy)-4-(4′-chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1312337-48-6);5-(Acetyloxy)-4-(2′,4′-dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one;5-(Acetyloxy)-4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1312340-82-1);5-(Acetyloxy)-4-(2′,4′-dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1033760-55-2);4-(4′-Chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1312337-51-1);4-(2′,4′-Dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester; 4-(4′-Chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1312340-83-2);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1033760-58-5); and non ACC herbicidessuch as benfuresate, butylate, cycloate, dalapon, dimepiperate, EPTC,esprocarb, ethofumesate, flupropanate, molinate, orbencarb, pebulate,prosulfocarb, TCA, thiobencarb, tiocarbazil, triallate and vernolate;

b2) from the group of the ALS inhibitors:

sulfonylureas such as amidosulfuron, azimsulfuron, bensulfuron,bensulfuron-methyl, chlorimuron, chlorimuron-ethyl, chlorsulfuron,cinosulfuron, cyclosulfamuron, ethametsulfuron, ethametsulfuron-methyl,ethoxysulfuron, flazasulfuron, flucetosulfuron, flupyrsulfuron,flupyrsulfuron-methyl-sodium, foramsulfuron, halosulfuron,halosulfuron-methyl, imazosulfuron, iodosulfuron,iodosulfuron-methyl-sodium, iofensulfuron, iofensulfuron-sodium,mesosulfuron, metazosulfuron, metsulfuron, metsulfuron-methyl,nicosulfuron, orthosulfamuron, oxasulfuron, primisulfuron,primisulfuron-methyl, propyrisulfuron, prosulfuron, pyrazosulfuron,pyrazosulfuron-ethyl, rimsulfuron, sulfometuron, sulfometuron-methyl,sulfosulfuron, thifensulfuron, thifensulfuron-methyl, triasulfuron,tribenuron, tribenuron-methyl, trifloxysulfuron, triflusulfuron,triflusulfuron-methyl and tritosulfuron,

imidazolinones such as imazamethabenz, imazamethabenz-methyl, imazamox,imazapic, imazapyr, imazaquin and imazethapyr, triazolopyrimidineherbicides and sulfonanilides such as cloransulam, cloransulam-methyl,diclosulam, flumetsulam, florasulam, metosulam, penoxsulam, pyrimisulfanand pyroxsulam, pyrimidinylbenzoates such as bispyribac,bispyribac-sodium, pyribenzoxim, pyriftalid, pyriminobac,pyriminobac-methyl, pyrithiobac, pyrithiobac-sodium,4-[[[2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]phenyl]methyl]amino]-benzoicacid-1-methylethyl ester (CAS 420138-41-6),4-[[[2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]phenyl]methyl]amino]-benzoicacid propyl ester (CAS 420138-40-5),N-(4-bromophenyl)-2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]benzenemethanamine(CAS 420138-01-8), sulfonylaminocarbonyl-triazolinone herbicides such asflucarbazone, flucarbazone-sodium, propoxycarbazone,propoxycarbazone-sodium, thiencarbazone and thiencarbazone-methyl; andtriafamone;

among these, a preferred embodiment of the invention relates to thosecompositions comprising at least one imidazolinone herbicide;

b3) from the group of the photosynthesis inhibitors:

amicarbazone, inhibitors of the photosystem II, e.g. triazineherbicides, including of chlorotriazine, triazinones, triazindiones,methylthiotriazines and pyridazinones such as ametryn, atrazine,chloridazone, cyanazine, desmetryn, dimethametryn,hexazinone,metribuzin, prometon, prometryn, propazine, simazine, simetryn,terbumeton, terbuthylazin, terbutryn and trietazin, aryl urea such aschlorobromuron, chlorotoluron, chloroxuron, dimefuron, diuron,fluometuron, isoproturon, isouron, linuron, metamitron,methabenzthiazuron, metobenzuron, metoxuron, monolinuron, neburon,siduron, tebuthiuron and thiadiazuron, phenyl carbamates such asdesmedipham, karbutilat, phenmedipham, phenmedipham-ethyl, nitrileherbicides such as bromofenoxim, bromoxynil and its salts and esters,ioxynil and its salts and esters, uraciles such as bromacil, lenacil andterbacil, and bentazon and bentazon-sodium, pyridate, pyridafol,pentanochlor and propanil and inhibitors of the photosystem I such asdiquat, diquat-dibromide, paraquat, paraquat-dichloride andparaquat-dimetilsulfate. Among these, a preferred embodiment of theinvention relates to those compositions comprising at least one arylurea herbicide. Among these, likewise a preferred embodiment of theinvention relates to those compositions comprising at least one triazineherbicide. Among these, likewise a preferred embodiment of the inventionrelates to those compositions comprising at least one nitrile herbicide;

b4) from the group of the protoporphyrinogen-IX oxidase inhibitors:

acifluorfen, acifluorfen-sodium, azafenidin, bencarbazone,benzfendizone, bifenox, butafenacil, carfentrazone, carfentrazone-ethyl,chlomethoxyfen, cinidon-ethyl, fluazolate, flufenpyr, flufenpyr-ethyl,flumiclorac, flumiclorac-pentyl, flumioxazin, fluoroglycofen,fluoroglycofen-ethyl, fluthiacet, fluthiacet-methyl, fomesafen,halosafen, lactofen, oxadiargyl, oxadiazon, oxyfluorfen, pentoxazone,profluazol, pyraclonil, pyraflufen, pyraflufen-ethyl, saflufenacil,sulfentrazone, thidiazimin, tiafenacil, trifludimoxazin (BAS 850 H),ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate(CAS 353292-31-6; S-3100; Sumitomo; LS 5296489),N-ethyl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452098-92-9),N-tetrahydrofurfuryl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 915396-43-9),N-ethyl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452099-05-7),N-tetrahydrofurfuryl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452100-03-7),3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl]-1,5-dimethyl-6-thioxo-[1,3,5]triazinan-2,4-dione(CAS 451484-50-7) (LS 4061013),2-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1,3-dione(CAS 1300118-96-0) (LS 567 0033=F2-Flumioxazin),1-methyl-6-trifluoromethyl-3-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-1H-pyrimidine-2,4-dione(CAS 1304113-05-0) (LS 568 1323=Uracil-F2-PPO), methyl(E)-4-[2-chloro-5-[4-chloro-5-(difluoromethoxy)-1H-methyl-pyrazol-3-yl]-4-fluoro-phenoxy]-3-methoxy-but-2-enoate (CAS948893-00-3) (Isagro, IR6396), and3-[7-chloro-5-fluoro-2-(trifluoromethyl)-1H-benzimidazol-4-yl]-1-methyl-6-(trifluoromethyl)-1H-pyrimidine-2,4-dione(CAS 212754-02-4) (FMC Trifluoromethyluracil);

b5) from the group of the bleacher herbicides:

PDS inhibitors: beflubutamid, diflufenican, fluridone, flurochloridone,flurtamone, norflurazon, picolinafen, and4-(3-trifluoromethylphenoxy)-2-(4-trifluoromethylphenyl)pyrimidine (CAS180608-33-7), HPPD inhibitors: benzobicyclon, benzofenap, bicyclopyrone,clomazone, fenquintrione, isoxaflutole, mesotrione, pyrasulfotole,pyrazolynate, pyrazoxyfen, sulcotrione, tefuryltrione, tembotrione,tolpyralate, topramezone, bleacher, unknown target: aclonifen, amitroleand flumeturon;

b6) from the group of the EPSP synthase inhibitors:

glyphosate, glyphosate-isopropylammonium, glyposate-potassium andglyphosate-trimesium (sulfosate);

b7) from the group of the glutamine synthase inhibitors:

bilanaphos (bialaphos), bilanaphos-sodium, glufosinate, glufosinate-Pand glufosinate-ammonium;

b8) from the group of the DHP synthase inhibitors:

asulam;

b9) from the group of the mitosis inhibitors:

compounds of group K1: dinitroanilines such as benfluralin, butralin,dinitramine, ethalfluralin, fluchloralin, oryzalin, pendimethalin,prodiamine and trifluralin, phosphoramidates such as amiprophos,amiprophos-methyl, and butamiphos, benzoic acid herbicides such aschlorthal, chlorthal-dimethyl, pyridines such as dithiopyr andthiazopyr, benzamides such as propyzamide and tebutam; compounds ofgroup K2: carbetamide, chlorpropham, flamprop, flamprop-isopropyl,flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl and propham;among these, compounds of group K1, in particular dinitroanilines arepreferred;

b10) from the group of the VLCFA inhibitors:

chloroacetamides such as acetochlor, alachlor, butachlor, dimethachlor,dimethenamid, dimethenamid-P, metazachlor, metolachlor, metolachlor-S,pethoxamid, pretilachlor, propachlor, propisochlor and thenylchlor,oxyacetanilides such as flufenacet and mefenacet, acetanilides such asdiphenamid, naproanilide, napropamide and napropamide-M, tetrazolinonessuch fentrazamide, and other herbicides such as anilofos, cafenstrole,fenoxasulfone, ipfencarbazone, piperophos, pyroxasulfone and isoxazolinecompounds of the formulae II.1, II.2, II.3, II.4, II.5, II.6, II.7, II.8and II.9

the isoxazoline compounds of the formula (I)I are known in the art, e.g.from WO 2006/024820, WO 2006/037945, WO 2007/071900 and WO 2007/096576;

among the VLCFA inhibitors, preference is given to chloroacetamides andoxyacetamides;

b11) from the group of the cellulose biosynthesis inhibitors:

chlorthiamid, dichlobenil, flupoxam, indaziflam, isoxaben, triaziflamand 1-cyclohexyl-5-pentafluorphenyloxy-1⁴-[1,2,4,6]thiatriazin-3-ylamine(CAS 175899-01-1);

b12) from the group of the decoupler herbicides:

dinoseb, dinoterb and DNOC and its salts;

b13) from the group of the auxinic herbicides:

2,4-D and its salts and esters such as clacyfos, 2,4-DB and its saltsand esters, aminocyclopyrachlor and its salts and esters, aminopyralidand its salts such as aminopyralid-dimethylammonium,aminopyralid-tris(2-hydroxypropyl)ammonium and its esters, benazolin,benazolin-ethyl, chloramben and its salts and esters, clomeprop,clopyralid and its salts and esters, dicamba and its salts and esters,dichlorprop and its salts and esters, dichlorprop-P and its salts andesters, fluroxypyr, fluroxypyr-butometyl, fluroxypyr-meptyl, halauxifenand its salts and esters (CAS 943832-60-8 DOW, LS 566509); MCPA and itssalts and esters, MCPA-thioethyl, MCPB and its salts and esters,mecoprop and its salts and esters, mecoprop-P and its salts and esters,picloram and its salts and esters, quinclorac, quinmerac, TBA (2,3,6)and its salts and esters, triclopyr and its salts and esters,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid (DOW, “Rinskor-acid”) and benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate(CAS 1390661-72-9) (DOW, “Rinskor”);

b14) from the group of the auxin transport inhibitors: diflufenzopyr,diflufenzopyr-sodium, naptalam and naptalam-sodium;

b15) from the group of the other herbicides: bromobutide, chlorflurenol,chlorflurenol-methyl, cinmethylin, cumyluron, cyclopyrimorate (CAS499223-49-3 Mitsui; SW-065; H-965) and its salts and esters, dalapon,dazomet, difenzoquat, difenzoquat-metilsulfate, dimethipin, DSMA,dymron, endothal and its salts, etobenzanid, flurenol, flurenol-butyl,flurprimidol, fosamine, fosamine-ammonium, indanofan, maleic hydrazide,mefluidide, metam, methiozolin (CAS 403640-27-7), methyl azide, methylbromide, methyl-dymron, methyl iodide, MSMA, oleic acid, oxaziclomefone,pelargonic acid, pyributicarb, quinoclamine and tridiphane.

Preferred herbicides B that can be used in combination with thediaminotriazine compounds of the formula (I) according to the presentinvention are:

b1) from the group of the lipid biosynthesis inhibitors:

clethodim, clodinafop-propargyl, cycloxydim, cyhalofop-butyl,diclofop-methyl, fenoxaprop-P-ethyl, fluazifop-P-butyl,haloxyfop-P-methyl, metamifop, pinoxaden, profoxydim, propaquizafop,quizalofop-P-ethyl, quizalofop-P-tefuryl, sethoxydim, tepraloxydim,tralkoxydim,4-(4′-Chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1312337-72-6);4-(2′,4′-Dichloro-4-cyclopropyl[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1312337-45-3);4-(4′-Chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1033757-93-5);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-2,2,6,6-tetramethyl-2H-pyran-3,5(4H,6H)-dione(CAS 1312340-84-3);5-(Acetyloxy)-4-(4′-chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1312337-48-6);5-(Acetyloxy)-4-(2′,4′-dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one;5-(Acetyloxy)-4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1312340-82-1);5-(Acetyloxy)-4-(2′,4′-dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1033760-55-2);4-(4′-Chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1312337-51-1);4-(2′,4′-Dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester;4-(4′-Chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1312340-83-2);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1033760-58-5); benfuresate,dimepiperate, EPTC, esprocarb, ethofumesate, molinate, orbencarb,prosulfocarb, thiobencarb and triallate;

b2) from the group of the ALS inhibitors:

amidosulfuron, azimsulfuron, bensulfuron-methyl, bispyribac-sodium,chlorimuron-ethyl, chlorsulfuron, cloransulam-methyl, cyclosulfamuron,diclosulam, ethametsulfuron-methyl, ethoxysulfuron, flazasulfuron,florasulam, flucarbazone-sodium, flucetosulfuron, flumetsulam,flupyrsulfuron-methyl-sodium, foramsulfuron, halosulfuron-methyl,imazamethabenz-methyl, imazamox, imazapic, imazapyr, imazaquin,imazethapyr, imazosulfuron, iodosulfuron, iodosulfuron-methyl-sodium,iofensulfuron, iofensulfuron-sodium, mesosulfuron, metazosulfuron,metosulam, metsulfuron-methyl, nicosulfuron, orthosulfamuron,oxasulfuron, penoxsulam, primisulfuron-methyl, propoxycarbazon-sodium,propyrisulfuron, prosulfuron, pyrazosulfuron-ethyl, pyribenzoxim,pyrimisulfan, pyriftalid, pyriminobac-methyl, pyrithiobac-sodium,pyroxsulam, rimsulfuron, sulfometuron-methyl, sulfosulfuron,thiencarbazone-methyl, thifensulfuron-methyl, triasulfuron,tribenuron-methyl, trifloxysulfuron, triflusulfuron-methyl,tritosulfuron and triafamone;

b3) from the group of the photosynthesis inhibitors:

ametryn, amicarbazone, atrazine, bentazone, bentazone-sodium, bromoxyniland its salts and esters, chloridazone, chlorotoluron, cyanazine,desmedipham, diquat-dibromide, diuron, fluometuron, hexazinone, ioxyniland its salts and esters, isoproturon, lenacil, linuron, metamitron,methabenzthiazuron, metribuzin, paraquat, paraquat-dichloride,phenmedipham, propanil, pyridate, simazine, terbutryn, terbuthylazineand thidiazuron;

b4) from the group of the protoporphyrinogen-IX oxidase inhibitors:

acifluorfen-sodium, bencarbazone, benzfendizone, butafenacil,carfentrazone-ethyl, cinidon-ethyl, flufenpyr-ethyl, flumiclorac-pentyl,flumioxazin, fluoroglycofen-ethyl, fomesafen, lactofen, oxadiargyl,oxadiazon, oxyfluorfen, pentoxazone, pyraflufen, pyraflufen-ethyl,saflufenacil, sulfentrazone, tiafenacil, trifludimoxazin (BAS 850 H),ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate(CAS 353292-31-6; S-3100; Sumitomo; LS 5296489),N-ethyl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452098-92-9),N-tetrahydrofurfuryl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 915396-43-9),N-ethyl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452099-05-7),N-tetrahydrofurfuryl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452100-03-7),3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl]-1,5-dimethyl-6-thioxo-[1,3,5]triazinan-2,4-dione(CAS 451484-50-7) (LS 4061013),2-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1,3-dione(CAS 1300118-96-0) (LS 567 0033=F2-Flumioxazin);1-methyl-6-trifluoromethyl-3-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-1H-pyrimidine-2,4-dione(CAS 1304113-05-0) (LS 568 1323=Uracil-F2-PPO), and3-[7-chloro-5-fluoro-2-(trifluoromethyl)-1H-benzimidazol-4-yl]-1-methyl-6-(trifluoromethyl)-1H-pyrimidine-2,4-dione(CAS 212754-02-4) (FMC Trifluoromethyluracil);

b5) from the group of the bleacher herbicides:

aclonifen, amitrole, beflubutamid, benzobicyclon, bicyclopyrone,clomazone, diflufenican, fenquintrione, flumeturon, flurochloridone,flurtamone, isoxaflutole, mesotrione, norflurazon, picolinafen,pyrasulfotole, pyrazolynate, sulcotrione, tefuryltrione, tembotrione,tolpyralate, topramezone and4-(3-trifluoromethylphenoxy)-2-(4-trifluoromethylphenyl)pyrimidine (CAS180608-33-7);

b6) from the group of the EPSP synthase inhibitors:

glyphosate, glyphosate-isopropylammonium, glyphosate-potassium andglyphosate-trimesium (sulfosate);

b7) from the group of the glutamine synthase inhibitors:

glufosinate, glufosinate-P, glufosinate-ammonium;

b8) from the group of the DHP synthase inhibitors: asulam;

b9) from the group of the mitosis inhibitors:

benfluralin, dithiopyr, ethalfluralin, flamprop, flamprop-isopropyl,flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl, oryzalin,pendimethalin, thiazopyr and trifluralin;

b10) from the group of the VLCFA inhibitors:

acetochlor, alachlor, anilofos, butachlor, cafenstrole, dimethenamid,dimethenamid-P, fentrazamide, flufenacet, mefenacet, metazachlor,metolachlor, S-metolachlor, naproanilide, napropamide, napropamide-M,pretilachlor, fenoxasulfone, ipfencarbazone, pyroxasulfone thenylchlorand isoxazoline-compounds of the formulae II.1, II.2, II.3, II.4, II.5,II.6, II.7, II.8 and II.9 as mentioned above;

b11) from the group of the cellulose biosynthesis inhibitors:dichlobenil, flupoxam, indaziflam, isoxaben, triaziflam and1-cyclohexyl-5-pentafluorphenyloxy-1⁴-[1,2,4,6]thiatriazin-3-ylamine(CAS 175899-01-1);

b13) from the group of the auxinic herbicides:

2,4-D and its salts and esters, aminocyclopyrachlor and its salts andesters, aminopyralid and its salts such asaminopyralid-dimethylammonium,aminopyralid-tris(2-hydroxypropyl)ammonium and its esters, clopyralidand its salts and esters, dicamba and its salts and esters,dichlorprop-P and its salts and esters, fluroxypyr-meptyl, halauxifenand its salts and esters (CAS 943832-60-8 DOW, LS 566509), MCPA and itssalts and esters, MCPB and its salts and esters, mecoprop-P and itssalts and esters, picloram and its salts and esters, quinclorac,quinmerac, triclopyr and its salts and esters,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid (DOW, “Rinskor-acid”) and benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate(CAS 1390661-72-9) (DOW, “Rinskor”);

b14) from the group of the auxin transport inhibitors: diflufenzopyr anddiflufenzopyr-sodium;

b15) from the group of the other herbicides: bromobutide, cinmethylin,cumyluron, cyclopyrimorate (CAS 499223-49-3 Mitsui; SW-065; H-965) andits salts and esters, dalapon, difenzoquat, difenzoquat-metilsulfate,DSMA, dymron (=daimuron), indanofan, metam, methylbromide, MSMA,oxaziclomefone, pyributicarb and tridiphane.

Particularly preferred herbicides B that can be used in combination withthe diaminotriazine compounds of the formula (I) according to thepresent invention are:

b1) from the group of the lipid biosynthesis inhibitors:clodinafop-propargyl, cycloxydim, cyhalofop-butyl, fenoxaprop-P-ethyl,pinoxaden, profoxydim, tepraloxydim, tralkoxydim,4-(4′-Chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1312337-72-6);4-(2′,4′-Dichloro-4-cyclopropyl[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1312337-45-3);4-(4′-Chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1033757-93-5);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-2,2,6,6-tetramethyl-2H-pyran-3,5(4H,6H)-dione(CAS 1312340-84-3);5-(Acetyloxy)-4-(4′-chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1312337-48-6);5-(Acetyloxy)-4-(2′,4′-dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one;5-(Acetyloxy)-4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1312340-82-1);5-(Acetyloxy)-4-(2′,4′-dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1033760-55-2);4-(4′-Chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1312337-51-1);4-(2′,4′-Dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester; 4-(4′-Chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1312340-83-2);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1033760-58-5); esprocarb, prosulfocarb,thiobencarb and triallate;

b2) from the group of the ALS inhibitors: bensulfuron-methyl,bispyribac-sodium, cyclosulfamuron, diclosulam, flumetsulam,flupyrsulfuron-methyl-sodium, foramsulfuron, imazamox, imazapic,imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron,iodosulfuron-methyl-sodium, iofensulfuron, iofensulfuron-sodium,mesosulfuron, metazosulfuron, nicosulfuron, penoxsulam,propoxycarbazon-sodium, propyrisulfuron, pyrazosulfuron-ethyl,pyroxsulam, rimsulfuron, sulfosulfuron, thiencarbazon-methyl,tritosulfuron and triafamone;

b3) from the group of the photosynthesis inhibitors: ametryn, atrazine,diuron, fluometuron, hexazinone, isoproturon, linuron, metribuzin,paraquat, paraquat-dichloride, propanil, terbutryn and terbuthylazine;

b4) from the group of the protoporphyrinogen-IX oxidase inhibitors:flumioxazin, oxyfluorfen, pyraflufen, pyraflufen-ethyl, saflufenacil,sulfentrazone, trifludimoxazin (BAS 850 H), ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate(CAS 353292-31-6; S-3100; Sumitomo; LS 5296489),3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl]-1,5-dimethyl-6-thioxo-[1,3,5]triazinan-2,4-dione(CAS 451484-50-7) (LS 4061013),2-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1,3-dione(CAS 1300118-96-0) (LS 567 0033=F2-Flumioxazin), and1-methyl-6-trifluoromethyl-3-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-1H-pyrimidine-2,4-dione(CAS 1304113-05-0) (LS 568 1323=Uracil-F2-PPO);

b5) from the group of the bleacher herbicides: amitrole, bicyclopyrone,clomazone, diflufenican, fenquintrione, flumeturon, flurochloridone,isoxaflutole, mesotrione, picolinafen, sulcotrione, tefuryltrione,tembotrione, tolpyralate and topramezone;

b6) from the group of the EPSP synthase inhibitors: glyphosate,glyphosate-isopropylammonium and glyphosate-trimesium (sulfosate);

b7) from the group of the glutamine synthase inhibitors: glufosinate,glufosinate-P and glufosinate-ammonium;

b9) from the group of the mitosis inhibitors: pendimethalin andtrifluralin;

b10) from the group of the VLCFA inhibitors: acetochlor, cafenstrole,dimethenamid-P, fentrazamide, flufenacet, mefenacet, metazachlor,metolachlor, S-metolachlor, fenoxasulfone, ipfencarbazone andpyroxasulfone; likewise, preference is given to isoxazoline compounds ofthe formulae II.1, II.2, II.3, II.4, II.5, II.6, II.7, II.8 and II.9 asmentioned above;

b11) from the group of the cellulose biosynthesis inhibitors:indaziflam, isoxaben and triaziflam;

b13) from the group of the auxinic herbicides: 2,4-D and its salts andesters such as clacyfos, and aminocyclopyrachlor and its salts andesters, aminopyralid and its salts and its esters, clopyralid and itssalts and esters, dicamba and its salts and esters, fluroxypyr-meptyl,halauxifen, halauxifen-methyl, quinclorac, quinmerac,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid (DOW, “Rinskor-acid”) and benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate(CAS 1390661-72-9) (DOW, “Rinskor”);

-   -   b14) from the group of the auxin transport inhibitors:        diflufenzopyr and diflufenzopyr-sodium,

b15) from the group of the other herbicides: dymron (=daimuron),indanofan, oxaziclomefone.

Particularly preferred herbicides B are the herbicides B as definedabove; in particular the herbicides B.1-B.196 listed below in table B:

TABLE B Herbicide B B.1 clethodim B.2 clodinafop-propargyl B.3cycloxydim B.4 cyhalofop-butyl B.5 fenoxaprop-ethyl B.6fenoxaprop-P-ethyl B.7 metamifop B.8 pinoxaden B.9 profoxydim B.10sethoxydim B.11 tepraloxydim B.12 tralkoxydim B.13 esprocarb B.14ethofumesate B.15 molinate B.16 prosulfocarb B.17 thiobencarb B.18triallate B.19 bensulfuron-methyl B.20 bispyribac-sodium B.21cloransulam-methyl B.22 chlorsulfuron B.23 clorimuron B.24cyclosulfamuron B.25 diclosulam B.26 florasulam B.27 flumetsulam B.28flupyrsulfuron-methyl-sodium B.29 foramsulfuron B.30 imazamox B.31imazamox-ammonium B.32 imazapic B.33 imazapic-ammonium B.34imazapic-isopropylammonium B.35 imazapyr B.36 imazapyr-ammonium B.37imazapyr-isopropylammonium B.38 imazaquin B.39 imazaquin-ammonium B.40imazethapyr B.41 imazethapyr-ammonium B.42 imazethapyr-isopropylammoniumB.43 imazosulfuron B.44 iodosulfuron-methyl-sodium B.45 iofensulfuronB.46 iofensulfuron-sodium B.47 mesosulfuron-methyl B.48 metazosulfuronB.49 metsulfuron-methyl B.50 metosulam B.51 nicosulfuron B.52 penoxsulamB.53 propoxycarbazon-sodium B.54 pyrazosulfuron-ethyl B.55 pyribenzoximB.56 pyriftalid B.57 pyroxsulam B.58 propyrisulfuron B.59 rimsulfuronB.60 sulfosulfuron B.61 thiencarbazone-methyl B.62 thifensulfuron-methylB.63 tribenuron-methyl B.64 tritosulfuron B.65 triafamone B.66 ametryneB.67 atrazine B.68 bentazon B.69 bromoxynil B.70 bromoxynil-octanoateB.71 bromoxynil-heptanoate B.72 bromoxynil-potassium B.73 diuron B.74fluometuron B.75 hexazinone B.76 isoproturon B.77 linuron B.78metamitron B.79 metribuzin B.80 propanil B.81 simazin B.82terbuthylazine B.83 terbutryn B.84 paraquat-dichloride B.85 acifluorfenB.86 butafenacil B.87 carfentrazone-ethyl B.88 flumioxazin B.89fomesafen B.90 oxadiargyl B.91 oxyfluorfen B.92 pyraflufen B.93pyraflufen-ethyl B.94 saflufenacil B.95 sulfentrazone B.96trifludimoxazin (BAS 850 H) B.97 ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate (CAS 353292-31-6) Sumitomo; LS 5296489 B.98benzobicyclon B.99 bicyclopyrone B.100 clomazone B.101 diflufenicanB.102 flurochloridone B.103 isoxaflutole B.104 mesotrione B.105norflurazone B.106 picolinafen B.107 sulcotrione B.108 tefuryltrioneB.109 tembotrione B.110 tolpyralate B.111 topramezone B.112topramezone-sodium B.113 amitrole B.114 fluometuron B.115 fenquintrioneB.116 glyphosate B.117 glyphosate-ammonium B.118glyphosate-dimethylammonium B.119 glyphosate-isopropylammonium B.120glyphosate-trimesium (sulfosate) B.121 glyphosate-potassium B.122glufosinate B.123 glufosinate-ammonium B.124 glufosinate-P B.125glufosinate-P-ammonium B.126 pendimethalin B.127 trifluralin B.128acetochlor B.129 butachlor B.130 cafenstrole B.131 dimethenamid-P B.132fentrazamide B.133 flufenacet B.134 mefenacet B.135 metazachlor B.136metolachlor B.137 S-metolachlor B.138 pretilachlor B.139 fenoxasulfoneB.140 indaziflam B.141 isoxaben B.142 triaziflam B.143 ipfencarbazoneB.144 pyroxasulfone B.145 2,4-D B.146 2,4-D-isobutyl B.1472,4-D-dimethylammonium B.148 2,4-D-N,N,N-trimethylethanolammonium B.149aminopyralid B.150 aminopyralid-methyl B.151aminopyralid-dimethyl-ammonium B.152aminopyralid-tris(2-hydroxypropyl)ammonium B.153 clopyralid B.154clopyralid-methyl B.155 clopyralid-olamine B.156 dicamba B.157dicamba-butotyl B.158 dicamba-diglycolamine B.159dicamba-dimethylammonium B.160 dicamba-diolamine B.161dicamba-isopropylammonium B.162 dicamba-potassium B.163 dicamba-sodiumB.164 dicamba-trolamine B.165 dicamba-N,N-bis-(3-aminopropyl)methylamineB.166 dicamba-diethylenetriamine B.167 fluroxypyr B.168fluroxypyr-meptyl B.169 halauxifen B.170 halauxifen-methyl B.171 MCPAB.172 MCPA-2-ethylhexyl B.173 MCPA-dimethylammonium B.174 quincloracB.175 quinclorac-dimethylammonium B.176 quinmerac B.177quinmerac-dimethylammonium B.1784-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylic acid (DOW, “Rinskor-acid”)B.179 benzyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxy-phenyl)-5-fluoropyridine-2-carboxylate (CAS 1390661-72- 9) (DOW,“Rinskor”) B.180 aminocyclopyrachlor B.181 aminocyclopyrachlor-potassiumB.182 aminocyclopyrachlor-methyl B.183 diflufenzopyr B.184diflufenzopyr-sodium B.185 dymron B.186 indanofan B.187 oxaziclomefoneB.188 II.1 B.189 II.2 B.190 II.3 B.191 II.4 B.192 II.5 B.193 II.6 B.194II.7 B.195 II.8 B.196 II.9

In another embodiment of the present invention the compositionsaccording to the present invention comprise at least one diaminotriazinecompound of formula (I) and at least one safener C.

Safeners are chemical compounds which prevent or reduce damage on usefulplants without having a major impact on the herbicidal action of theherbicidal active components of the present compositions towardsunwanted plants. They can be applied either before sowings (e.g. on seedtreatments, shoots or seedlings) or in the pre-emergence application orpost-emergence application of the useful plant. The safeners and thediaminotriazine compound of formula (I) and/or the herbicides B can beapplied simultaneously or in succession.

Suitable safeners are e.g. (quinolin-8-oxy)acetic acids,1-phenyl-5-haloalkyl-1H-1,2,4-triazol-3-carboxylic acids,1-phenyl-4,5-dihydro-5-alkyl-1H-pyrazol-3,5-dicarboxylic acids,4,5-dihydro-5,5-diaryl-3-isoxazol carboxylic acids, dichloroacetamides,alpha-oximinophenylacetonitriles, acetophenonoximes,4,6-dihalo-2-phenylpyrimidines,N-[[4-(aminocarbonyl)phenyl]sulfonyl]-2-benzoic amides, 1,8-naphthalicanhydride, 2-halo-4-(haloalkyl)-5-thiazol carboxylic acids,phosphorthiolates and N-alkyl-O-phenylcarbamates and theiragriculturally acceptable salts and their agriculturally acceptablederivatives such amides, esters, and thioesters, provided they have anacid group.

Examples of preferred safeners C are benoxacor, cloquintocet,cyometrinil, cyprosulfamide, dichlormid, dicyclonon, dietholate,fenchlorazole, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen,mefenpyr, mephenate, naphthalic anhydride, oxabetrinil,4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (MON4660, CAS71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine(R-29148, CAS 52836-31-4) and N-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide (CAS129531-12-0).

Especially preferred safeners C are benoxacor, cloquintocet,cyprosulfamide, dichlormid, fenchlorazole, fenclorim, flurazole,fluxofenim, furilazole, isoxadifen, mefenpyr, naphthalic anhydride,oxabetrinil, 4-(dichloroacetyl)-1-oxa-4-azaspiro-[4.5]decane (MON4660,CAS 71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine(R-29148, CAS 52836-31-4) andN-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide(CAS 129531-12-0).

Particularly preferred safeners C are benoxacor, cloquintocet,cyprosulfamide, dichlormid, fenchlorazole, fenclorim, furilazole,isoxadifen, mefenpyr, naphtalic anhydride,4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (MON4660, CAS71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine(R-29148, CAS 52836-31-4) and N-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide (CAS129531-12-0).

Particularly preferred safeners C, which, as component C, areconstituent of the composition according to the invention are thesafeners C as defined above; in particular the safeners C.1-C.17 listedbelow in table C:

TABLE C Safener C C.1 benoxacor C.2 cloquintocet C.3 cloquintocet-mexylC.4 cyprosulfamide C.5 dichlormid C.6 fenchlorazole C.7fenchlorazole-ethyl C.8 fenclorim C.9 furilazole C.10 isoxadifen C.11isoxadifen-ethyl C.12 mefenpyr C.13 mefenpyr-diethyl C.14 naphtalic acidanhydride C.15 4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (MON4660,CAS 71526-07-3) C.16 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine(R-29148, CAS 52836-31-4) C.17N-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzene- sulfonamide(CAS 129531-12-0)The active compounds B of groups b1) to b15) and the active compounds Care known herbicides and safeners, see, for example, The Compendium ofPesticide Common Names (http://www.alanwood.net/pesticides/); FarmChemicals Handbook 2000 volume 86, Meister Publishing Company, 2000; B.Hock, C. Fedtke, R. R. Schmidt, Herbizide [Herbicides], Georg ThiemeVerlag, Stuttgart 1995; W. H. Ahrens, Herbicide Handbook, 7th edition,Weed Science Society of America, 1994; and K. K. Hatzios, HerbicideHandbook, Supplement for the 7th edition, Weed Science Society ofAmerica, 1998. 2,2,5-Trimethyl-3-(dichloroacetyl)-1,3-oxazolidine [CASNo. 52836-31-4] is also referred to as R-29148.4-(Dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane [CAS No. 71526-07-3] isalso referred to as AD-67 and MON 4660.

The assignment of the active compounds to the respective mechanisms ofaction is based on current knowledge. If several mechanisms of actionapply to one active compound, this substance was only assigned to onemechanism of action.

Active compounds B and C having a carboxyl group can be employed in theform of the acid, in the form of an agriculturally suitable salt asmentioned above or else in the form of an agriculturally acceptablederivative in the compositions according to the invention.

In the case of dicamba, suitable salts include those, where thecounterion is an agriculturally acceptable cation. For example, suitablesalts of dicamba are dicamba-sodium, dicamba-potassium,dicamba-methylammonium, dicamba-dimethylammonium,dicamba-isopropylammonium, dicamba-diglycolamine, dicamba-olamine,dicamba-diolamine, dicamba-trolamine,dicamba-N,N-bis-(3-aminopropyl)methylamine anddicamba-diethylenetriamine. Examples of a suitable ester aredicamba-methyl and dicamba-butotyl.

Suitable salts of 2,4-D are 2,4-D-ammonium, 2,4-D-dimethylammonium,2,4-D-diethylammonium, 2,4-D-diethanolammonium (2,4-D-diolamine),2,4-D-triethanol-ammonium, 2,4-D-isopropylammonium,2,4-D-triisopropanolammonium, 2,4-D-heptylammonium,2,4-D-dodecylammonium, 2,4-D-tetradecylammonium, 2,4-D-triethylammonium,2,4-D-tris(2-hydroxypropyl)ammonium, 2,4-D-tris(isopropyl)-ammonium,2,4-D-trolamine, 2,4-D-lithium, 2,4-D-sodium. Examples of suitableesters of 2,4-D are 2,4-D-butotyl, 2,4-D-2-butoxypropyl,2,4-D-3-butoxypropyl, 2,4-D-butyl, 2,4-D-ethyl, 2,4-D-ethylhexyl,2,4-D-isobutyl, 2,4-D-isooctyl, 2,4-D-isopropyl, 2,4-D-meptyl,2,4-D-methyl, 2,4-D-octyl, 2,4-D-pentyl, 2,4-D-propyl, 2,4-D-tefuryl andclacyfos.

Suitable salts of 2,4-DB are for example 2,4-DB-sodium, 2,4-DB-potassiumand 2,4-DB-dimethylammonium. Suitable esters of 2,4-DB are for example2,4-DB-butyl and 2,4-DB-isoctyl.

Suitable salts of dichlorprop are for example dichlorprop-sodium,dichlorprop-potassium and dichlorprop-dimethylammonium. Examples ofsuitable esters of dichlorprop are dichlorprop-butotyl anddichlorprop-isoctyl.

Suitable salts and esters of MCPA include MCPA-butotyl, MCPA-butyl,MCPA-dimethylammonium, MCPA-diolamine, MCPA-ethyl, MCPA-thioethyl,MCPA-2-ethylhexyl, MCPA-isobutyl, MCPA-isoctyl, MCPA-isopropyl,MCPA-isopropylammonium, MCPA-methyl, MCPA-olamine, MCPA-potassium,MCPA-sodium and MCPA-trolamine.

A suitable salt of MCPB is MCPB sodium. A suitable ester of MCPB isMCPB-ethyl.

Suitable salts of clopyralid are clopyralid-potassium,clopyralid-olamine and clopyralid-tris-(2-hydroxypropyl)ammonium.Example of suitable esters of clopyralid is clopyralid-methyl.

Examples of a suitable ester of fluroxypyr are fluroxypyr-meptyl andfluroxypyr-2-butoxy-1-methylethyl, wherein fluroxypyr-meptyl ispreferred.

Suitable salts of picloram are picloram-dimethylammonium,picloram-potassium, picloram-triisopropanolammonium,picloram-triisopropylammonium and picloram-trolamine. A suitable esterof picloram is picloram-isoctyl.

A suitable salt of triclopyr is triclopyr-triethylammonium. Suitableesters of triclopyr are for example triclopyr-ethyl andtriclopyr-butotyl.

Suitable salts and esters of chloramben include chloramben-ammonium,chloramben-diolamine, chloramben-methyl, chloramben-methylammonium andchloramben-sodium. Suitable salts and esters of 2,3,6-TBA include2,3,6-TBA-dimethylammonium, 2,3,6-TBA-lithium, 2,3,6-TBA-potassium and2,3,6-TBA-sodium.

Suitable salts and esters of aminopyralid includeaminopyralid-potassium, aminopyralid-dimethylammonium, andaminopyralid-tris(2-hydroxypropyl)ammonium.

Suitable salts of glyphosate are for example glyphosate-ammonium,glyphosate-diammonium, glyphoste-dimethylammonium,glyphosate-isopropylammonium, glyphosate-potassium, glyphosate-sodium,glyphosate-trimesium as well as the ethanolamine and diethanolaminesalts, preferably glyphosate-diammonium, glyphosate-isopropylammoniumand glyphosate-trimesium (sulfosate).

A suitable salt of glufosinate is for example glufosinate-ammonium.

A suitable salt of glufosinate-P is for example glufosinate-P-ammonium.

Suitable salts and esters of bromoxynil are for examplebromoxynil-butyrate, bromoxynil-heptanoate, bromoxynil-octanoate,bromoxynil-potassium and bromoxynil-sodium.

Suitable salts and esters of ioxonil are for example ioxonil-octanoate,ioxonil-potassium and ioxonil-sodium.

Suitable salts and esters of mecoprop include mecoprop-butotyl,mecoprop-dimethylammonium, mecoprop-diolamine, mecoprop-ethadyl,mecoprop-2-ethylhexyl, mecoprop-isoctyl, mecoprop-methyl,mecoprop-potassium, mecoprop-sodium and mecoprop-trolamine.

Suitable salts of mecoprop-P are for example mecoprop-P-butotyl,mecoprop-P-dimethylammonium, mecoprop-P-2-ethylhexyl,mecoprop-P-isobutyl, mecoprop-P-potassium and mecoprop-P-sodium.

A suitable salt of diflufenzopyr is for example diflufenzopyr-sodium.

A suitable salt of naptalam is for example naptalam-sodium.

Suitable salts and esters of aminocyclopyrachlor are for exampleaminocyclopyrachlor-dimethylammonium, aminocyclopyrachlor-methyl,aminocyclopyrachlor-triisopropanolammonium, aminocyclopyrachlor-sodiumand aminocyclopyrachlor-potassium.

A suitable salt of quinclorac is for examplequinclorac-dimethylammonium.

A suitable salt of quinmerac is for example quinmerac-dimethylammonium.

A suitable salt of imazamox is for example imazamox-ammonium.

Suitable salts of imazapic are for example imazapic-ammonium andimazapic-isopropylammonium.

Suitable salts of imazapyr are for example imazapyr-ammonium andimazapyr-isopropylammonium.

A suitable salt of imazaquin is for example imazaquin-ammonium.

Suitable salts of imazethapyr are for example imazethapyr-ammonium andimazethapyr-isopropylammonium.

A suitable salt of topramezone is for example topramezone-sodium.

According to a preferred embodiment of the invention, the compositioncomprises as herbicidal active compound B or component B at least one,preferably exactly one herbicide B.

According to another preferred embodiment of the invention, thecomposition comprises as herbicidal active compounds B or component B atleast two, preferably exactly two herbicides B different from eachother.

According to another preferred embodiment of the invention, thecomposition comprises as herbicidal active compounds B or component B atleast three, preferably exactly three herbicides B different from eachother.

According to another preferred embodiment of the invention, thecomposition comprises as safening component C or component C at leastone, preferably exactly one safener C.

According to another preferred embodiment of the invention, thecomposition comprises as component B at least one, preferably exactlyone herbicide B, and as component C at least one, preferably exactlyone, safener C.

According to another preferred embodiment of the invention, thecomposition comprises at least two, preferably exactly two, herbicides Bdifferent from each other, and as component C at least one, preferablyexactly one, safener C.

According to another preferred embodiment of the invention, thecomposition comprises at least three, preferably exactly three,herbicides B different from each other, and as component C at least one,preferably exactly one, safener C.

According to another preferred embodiment of the invention, thecomposition comprises at least one, preferably exactly one compound offormula (I) and as component B at least one, preferably exactly one,herbicide B.

According to another preferred embodiment of the invention, thecomposition comprises at least one, preferably exactly one compound offormula (I) and at least two, preferably exactly two, herbicides Bdifferent from each other.

According to another preferred embodiment of the invention, thecomposition comprises at least one, preferably exactly one compound offormula (I) and at least three, preferably exactly three, herbicides Bdifferent from each other.

According to another preferred embodiment of the invention, thecomposition comprises at least one, preferably exactly one compound offormula (I) and as component C at least one, preferably exactly one,safener C.

According to another preferred embodiment of the invention, thecomposition comprises at least one, preferably exactly one compound offormula (I) as component B at least one, preferably exactly one,herbicide B, and as component C at least one, preferably exactly onesafener C.

According to another preferred embodiment of the invention, thecomposition comprises at least one, preferably exactly one compound offormula (I), at least two, preferably exactly two herbicides B differentfrom each other, and as component C at least one, preferably exactlyone, safener C.

According to another preferred embodiment of the invention, thecomposition comprises at least one, preferably exactly one compound offormula (I) at least three, preferably exactly three herbicides Bdifferent from each other, and as component C at least one, preferablyexactly one, safener C.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b1), in particular selected from the group consisting ofclodinafop-propargyl, cycloxydim, cyhalofop-butyl, fenoxaprop-P-ethyl,pinoxaden, profoxydim, tepraloxydim, tralkoxydim, esprocarb,prosulfocarb, thiobencarb and triallate.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b2), in particular selected from the group consisting ofbensulfuron-methyl, bispyribac-sodium, cyclosulfamuron, diclosulam,flumetsulam, flupyrsulfuron-methyl-sodium, foramsulfuron, imazamox,imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron,iodosulfuron-methyl-sodium, mesosulfuron, metazosulfuron, nicosulfuron,penoxsulam, propoxycarbazon-sodium, pyrazosulfuron-ethyl, pyroxsulam,rimsulfuron, sulfosulfuron, thiencarbazon-methyl and tritosulfuron.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b3), in particular selected from the group consisting of ametryn,atrazine, diuron, fluometuron, hexazinone, isoproturon, linuron,metribuzin, paraquat, paraquat-dichloride, propanil, terbutryn andterbuthylazine.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b4), in particular selected from the group consisting offlumioxazin, oxyfluorfen, pyraflufen, pyraflufen-ethyl, saflufenacil,sulfentrazone, trifludimoxazin (BAS 850 H), ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate(CAS 353292-31-6; S-3100; Sumitomo; LS 5296489),3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl]-1,5-dimethyl-6-thioxo-[1,3,5]triazinan-2,4-dione(CAS 451484-50-7) LS 4061013),2-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1,3-dione(CAS 1300118-96-0) (LS 567 0033=F2-Flumioxazin) and1-methyl-6-trifluoromethyl-3-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-1H-pyrimidine-2,4-dione(CAS 1304113-05-0) (LS 568 1323=Uracil-F2-PPO).

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b5), in particular selected from the group consisting of amitrole,bicyclopyrone, clomazone, diflufenican, flumeturon, flurochloridone,isoxaflutole, mesotrione, picolinafen, sulcotrione, tefuryltrione,tembotrione, tolpyralate and topramezone.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b6), in particular selected from the group consisting ofglyphosate, glyphosate-isopropylammonium and glyphosate-trimesium(sulfosate).

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b7), in particular selected from the group consisting ofglufosinate, glufosinate-P and glufosinate-ammonium.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b9), in particular selected from the group consisting ofpendimethalin and trifluralin.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b10), in particular selected from the group consisting ofacetochlor, cafenstrole, dimethenamid-P, fentrazamide, flufenacet,mefenacet, metazachlor, metolachlor, S-metolachlor, fenoxasulfone andpyroxasulfone. Likewise, preference is given to compositions comprisingin addition to a compounds of formula (I), at least one and especiallyexactly one herbicidally active compound from group b10), in particularselected from the group consisting of isoxazoline compounds of theformulae II.1, II.2, II.3, II.4, II.5, II.6, II.7, II.8 and II.9, asdefined above.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b11), in particular indaziflam, isoxaben and triaziflam.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b13), in particular selected from the group consisting of 2,4-Dand its salts and esters, aminocyclopyrachlor and its salts and esters,aminopyralid and its salts such as aminopyralid-dimethylammonium,aminopyralid-tris(2-hydroxypropyl)ammonium and its esters, clopyralidand its salts and esters, dicamba and its salts and esters,fluroxypyr-meptyl, halauxifen, halauxifen-methyl, quinclorac, quinmerac,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid (DOW, “Rinskor-acid”) and benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate(CAS 1390661-72-9) (DOW, “Rinskor”).

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b14), in particular selected from the group consisting ofdiflufenzopyr and diflufenzopyr-sodium.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one herbicidally active compound fromgroup b15), in particular selected from the group consisting of dymron(=daimuron), indanofan and oxaziclomefone.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to a compounds of formula (I), atleast one and especially exactly one safener C, in particular selectedfrom the group consisting of benoxacor, cloquintocet, cyprosulfamide,dichlormid, fenchlorazole, fenclorim, furilazole, isoxadifen, mefenpyr,4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (MON4660, CAS 71526-07-3)and 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine (R-29148, CAS52836-31-4).

Further preferred embodiments relate to ternary compositions whichcorrespond to the binary compositions mentioned above and additionallycomprise a safener C, in particular selected from the group consistingof benoxacor, cloquintocet, cyprosulfamide, dichlormid, fenchlorazole,fenclorim, furilazole, isoxadifen, mefenpyr,4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (MON4660, CAS 71526-07-3)and 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine (R-29148, CAS52836-31-4).

Here and below, the term “binary compositions” includes compositionscomprising one or more, for example 1, 2 or 3, active compounds of theformula (I) and either one or more, for example 1, 2 or 3, herbicides Bor one or more safeners C.

Correspondingly, the term “ternary compositions” includes compositionscomprising one or more, for example 1, 2 or 3, active compounds of theformula (I), one or more, for example 1, 2 or 3, herbicides B and one ormore, for example 1, 2 or 3, safeners C.

In binary compositions comprising at least one compound of the formula(I) as component A and at least one herbicide B, the weight ratio of theactive compounds A:B is generally in the range of from 1:1000 to 1000:1,preferably in the range of from 1:500 to 500:1, in particular in therange of from 1:250 to 250:1 and particularly preferably in the range offrom 1:75 to 75:1.

In binary compositions comprising at least one compound of the formula(I) as component A and at least one safener C, the weight ratio of theactive compounds A:C is generally in the range of from 1:1000 to 1000:1,preferably in the range of from 1:500 to 500:1, in particular in therange of from 1:250 to 250:1 and particularly preferably in the range offrom 1:75 to 75:1.

In ternary compositions comprising at least one compound of formula (I)as component A, at least one herbicide B and at least one safener C, therelative proportions by weight of the components A:B are generally inthe range of from 1:1000 to 1000:1, preferably in the range of from1:500 to 500:1, in particular in the range of from 1:250 to 250:1 andparticularly preferably in the range of from 1:75 to 75:1, the weightratio of the components A:C is generally in the range of from 1:1000 to1000:1, preferably in the range of from 1:500 to 500:1, in particular inthe range of from 1:250 to 250:1 and particularly preferably in therange of from 1:75 to 75:1, and the weight ratio of the components B:Cis generally in the range of from 1:1000 to 1000:1, preferably in therange of from 1:500 to 500:1, in particular in the range of from 1:250to 250:1 and particularly preferably in the range of from 1:75 to 75:1.The weight ratio of components A+B to component C is preferably in therange of from 1:500 to 500:1, in particular in the range of from 1:250to 250:1 and particularly preferably in the range of from 1:75 to 75:1.

The weight ratios of the individual components in the preferred mixturesmentioned below are within the limits given above, in particular withinthe preferred limits.

Particularly preferred are the compositions mentioned below comprisingthe compounds of formula (I) as defined and the substance(s) as definedin the respective row of table 1;

especially preferred comprising as only herbicidal active compounds thecompounds of formula (I) as defined and the substance(s) as defined inthe respective row of table 1;

most preferably comprising as only active compounds the compounds offormula I as defined and the substance(s) as defined in the respectiverow of table 1.

Particularly preferred are compositions 1.1 to 1.3545, comprising thecompounds of formula (I) and the substance(s) as defined in therespective row of table 1:

The following combinations indicated by the code A-X.Y.Z representparticular embodiments of the invention:

A-1.1.1 to A-1.256.3545, A-2.1.1 to A-2.256.3545, A-3.1.1 toA-3.256.3545, A-4.1.1 to A-4.256.3545, A-5.1.1 to A-5.256.3545, A-6.1.1to A-6.256.3545, A-7.1.1 to A-7.256.3545, A-8.1.1 to A-8.256.3545,A-9.1.1 to A-9.256.3545, A-10.1.1 to A-10.256.3545, A-11.1.1 toA-11.256.3545, A-12.1.1 to A-12.256.3545, A-13.1.1 to A-13.256.3545,A-14.1.1 to A-14.256.3545, A-15.1.1 to A-15.256.3545, A-16.1.1 toA-16.256.3545, A-17.1.1 to A-17.256.3545, A-18.1.1 to A-18.256.3545,A-19.1.1 to A-19.256.3545, A-20.1.1 to A-20.256.3545, A-21.1.1 toA-21.256.3545, A-22.1.1 to A-22.256.3545, A-23.1.1 to A-23.256.3545,A-24.1.1 to A-24.256.3545, A-25.1.1 to A-25.256.3545, A-26.1.1 toA-26.256.3545, A-27.1.1 to A-27.256.3545, A-28.1.1 to A-28.256.3545,A-29.1.1 to A-29.256.3545, A-30.1.1 to A-30.256.3545, A-31.1.1 toA-31.256.3545, A-32.1.1 to A-32.256.3545, A-33.1.1 to A-33.256.3545,A-34.1.1 to A-34.256.3545, A-35.1.1 to A-35.256.3545, A-36.1.1 toA-36.256.3545, A-37.1.1 to A-37.256.3545, A-38.1.1 to A-38.256.3545,A-39.1.1 to A-39.256.3545, A-40.1.1 to A-40.256.3545, A-41.1.1 toA-41.256.3545, A-42.1.1 to A-42.256.3545, A-43.1.1 to A-43.256.3545,A-44.1.1 to A-44.256.3545, A-45.1.1 to A-45.256.3545, A-46.1.1 toA-46.256.3545, A-47.1.1 to A-47.256.3545, A-48.1.1 to A-48.256.3545,A-49.1.1 to A-49.256.3545, A-50.1.1 to A-50.256.3545, A-51.1.1 toA-51.256.3545, A-52.1.1 to A-52.256.3545, A-53.1.1 to A-53.256.3545,A-54.1.1 to A-54.256.3545, A-55.1.1 to A-55.256.3545, A-56.1.1 toA-56.256.3545, A-57.1.1 to A-57.256.3545, A-58.1.1 to A-58.256.3545,A-59.1.1 to A-59.256.3545, A-60.1.1 to A-60.256.3545, A-61.1.1 toA-61.256.3545, A-62.1.1 to A-62.256.3545, A-63.1.1 to A-63.256.3545,A-64.1.1 to A-64.256.3545, A-65.1.1 to A-65.256.3545, A-66.1.1 toA-66.256.3545, A-67.1.1 to A-67.256.3545, A-68.1.1 to A-68.256.3545,A-69.1.1 to A-69.256.3545, A-70.1.1 to A-70.256.3545, A-71.1.1 toA-71.256.3545, A-72.1.1 to A-72.256.3545, A-73.1.1 to A-73.256.3545,A-74.1.1 to A-74.256.3545, A-75.1.1 to A-75.256.3545, A-76.1.1 toA-76.256.3545, A-77.1.1 to A-77.256.3545, A-78.1.1 to A-78.256.3545,A-79.1.1 to A-79.256.3545, A-80.1.1 to A-80.256.3545.

In the above codes A-X refers to the numbers of tables A-1 to A.80. Theinteger Y refers to the row of table A, while the integer Z refers tothe row of table 1 below.

Hence, the code A-1.1.1 refers to the combination of the compound offormula I.a of table A-1, wherein R², R³, R⁴ and R⁵ are as defined inrow 1 of table A, with the combination of the herbicide B and and thesafener C are as defined in combination no. 1.1 of table 1.

The code A-12.2.35 refers to the combination of the compound of formulaI.a of table A-12, wherein R², R³, R⁴ and R⁵ are as defined in row 2 oftable A, with the combination of the herbicide B and and the safener Care as defined in combination no. 1.35 of table 1.

The code A-35.256.3545 refers to the combination of the compound offormula I.a of table A-35, wherein R², R³, R⁴ and R⁵ are as defined inrow 256 of table A, with the combination of the herbicide B and and thesafener C are as defined in combination no. 1.3545 of table 1.

Further particluar examples are the following mixtures:

-   -   mixtures A-9.1.1 to A-9.1.3545, i.e. the mixtures of the        compound of table A-9, where R², R³, R⁴ and R⁵ are as defined in        row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-10.1.1 to A-10.1.3545, i.e. the mixtures of the        compound of table A-10, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-16.1.1 to A-16.1.3545, i.e. the mixtures of the        compound of table A-16, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-17.1.1 to A-17.1.3545, i.e. the mixtures of the        compound of table A-17, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-18.1.1 to A-18.1.3545, i.e. the mixtures of the        compound of table A-18, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-24.1.1 to A-24.1.3545, i.e. the mixtures of the        compound of table A-24, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-25.1.1 to A-25.1.3545, i.e. the mixtures of the        compound of table A-25, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-26.1.1 to A-26.1.3545, i.e. the mixtures of the        compound of table A-26, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-32.1.1 to A-32.1.3545, i.e. the mixtures of the        compound of table A-32, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-33.1.1 to A-33.1.3545, i.e. the mixtures of the        compound of table A-33, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-34.1.1 to A-34.1.3545, i.e. the mixtures of the        compound of table A-34, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-40.1.1 to A-40.1.3545, i.e. the mixtures of the        compound of table A-40, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-57.1.1 to A-57.1.3545, i.e. the mixtures of the        compound of table A-57, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-58.1.1 to A-58.1.3545, i.e. the mixtures of the        compound of table A-58, where R², R³, R⁴ and R⁵ X are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-64.1.1 to A-64.1.3545, i.e. the mixtures of the        compound of table A-64, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-65.1.1 to A-65.1.3545, i.e. the mixtures of the        compound of table A-65, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-66.1.1 to A-66.1.3545, i.e. the mixtures of the        compound of table A-66, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-72.1.1 to A-27.1.3545, i.e. the mixtures of the        compound of table A-72, where R², R³, R⁴ and R⁵ are as defined        in row 1 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.13.1 to A-1.13.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 13 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.15.1 to A-1.15.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 15 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.19.1 to A-1.19.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 19 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.22.1 to A-1.22.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 22 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.25.1 to A-1.25.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 25 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.38.1 to A-1.38.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 38 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.39.1 to A-1.39.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 39 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.42.1 to A-1.42.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 42 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.43.1 to A-1.43.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 43 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.46.1 to A-1.46.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 46 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.47.1 to A-1.47.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 47 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.53.1 to A-1.53.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 53 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-1.55.1 to A-1.55.3545, i.e. the mixtures of the        compound of table A-i, where R², R³, R⁴ and R⁵ are as defined in        row 55 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.13.1 to A-2.13.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 13 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.15.1 to A-2.15.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 15 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.19.1 to A-2.19.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 19 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.22.1 to A-2.22.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 22 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.25.1 to A-2.25.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 25 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.38.1 to A-2.38.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 38 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.39.1 to A-2.39.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 39 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.42.1 to A-2.42.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 42 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.43.1 to A-2.43.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 43 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.46.1 to A-2.46.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 46 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.47.1 to A-2.47.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 47 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.53.1 to A-2.53.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 53 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-2.55.1 to A-2.55.3545, i.e. the mixtures of the        compound of table A-2, where R², R³, R⁴ and R⁵ are as defined in        row 55 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.13.1 to A-8.13.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 13 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.15.1 to A-8.15.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 15 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.19.1 to A-8.19.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 19 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.22.1 to A-8.22.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 22 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.25.1 to A-8.25.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 25 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.38.1 to A-8.38.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 38 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.39.1 to A-8.39.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 39 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.42.1 to A-8.42.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 42 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.43.1 to A-8.43.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 43 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.46.1 to A-8.46.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 46 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.47.1 to A-8.47.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 47 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.53.1 to A-8.53.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 53 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;    -   mixtures A-8.55.1 to A-8.55.3545, i.e. the mixtures of the        compound of table A-8, where R², R³, R⁴ and R⁵ are as defined in        row 55 of table A and where the herbicide or herbicide safener        combination is as defined in one of the rows 1.1 to 1.3545 of        table 1;

TABLE 1 (compositions 1.1 to 1.3545): comp. no. herbicide B safener C1.1 B.1 — 1.2 B.2 — 1.3 B.3 — 1.4 B.4 — 1.5 B.5 — 1.6 B.6 — 1.7 B.7 —1.8 B.8 — 1.9 B.9 — 1.10 B.10 — 1.11 B.11 — 1.12 B.12 — 1.13 B.13 — 1.14B.14 — 1.15 B.15 — 1.16 B.16 — 1.17 B.17 — 1.18 B.18 — 1.19 B.19 — 1.20B.20 — 1.21 B.21 — 1.22 B.22 — 1.23 B.23 — 1.24 B.24 — 1.25 B.25 — 1.26B.26 — 1.27 B.27 — 1.28 B.28 — 1.29 B.29 — 1.30 B.30 — 1.31 B.31 — 1.32B.32 — 1.33 B.33 — 1.34 B.34 — 1.35 B.35 — 1.36 B.36 — 1.37 B.37 — 1.38B.38 — 1.39 B.39 — 1.40 B.40 — 1.41 B.41 — 1.42 B.42 — 1.43 B.43 — 1.44B.44 — 1.45 B.45 — 1.46 B.46 — 1.47 B.47 — 1.48 B.48 — 1.49 B.49 — 1.50B.50 — 1.51 B.51 — 1.52 B.52 — 1.53 B.53 — 1.54 B.54 — 1.55 B.55 — 1.56B.56 — 1.57 B.57 — 1.58 B.58. — 1.59 B.59 — 1.60 B.60 — 1.61 B.61 — 1.62B.62 — 1.63 B.63 — 1.64 B.64 — 1.65 B.65 — 1.66 B.66 — 1.67 B.67 — 1.68B.68 — 1.69 B.69 — 1.70 B.70 — 1.71 B.71 — 1.72 B.72 — 1.73 B.73 — 1.74B.74 — 1.75 B.75 — 1.76 B.76 — 1.77 B.77 — 1.78 B.78 — 1.79 B.79 — 1.80B.80 — 1.81 B.81 — 1.82 B.82 — 1.83 B.83 — 1.84 B.84 — 1.85 B.85 — 1.86B.86 — 1.87 B.87 — 1.88 B.88 — 1.89 B.89 — 1.90 B.90 — 1.91 B.91 — 1.92B.92 — 1.93 B.93 — 1.94 B.94 — 1.95 B.95 — 1.96 B.96 — 1.97 B.97 — 1.98B.98 — 1.99 B.99 — 1.100 B.100 — 1.101 B.101 — 1.102 B.102 — 1.103 B.103— 1.104 B.104 — 1.105 B.105 — 1.106 B.106 — 1.107 B.107 — 1.108 B.108 —1.109 B.109 — 1.110 B.110 — 1.111 B.111 — 1.112 B.112 — 1.113 B.113 —1.114 B.114 — 1.115 B.115 — 1.116 B.116 — 1.117 B.117 — 1.118 B.118 —1.119 B.119 — 1.120 B.120 — 1.121 B.121 — 1.122 B.122 — 1.123 B.123 —1.124 B.124 — 1.125 B.125 — 1.126 B.126 — 1.127 B.127 — 1.128 B.128 —1.129 B.129 — 1.130 B.130 — 1.131 B.131 — 1.132 B.132 — 1.133 B.133 —1.134 B.134 — 1.135 B.135 — 1.136 B.136 — 1.137 B.137 — 1.138 B.138 —1.139 B.139 — 1.140 B.140 — 1.141 B.141 — 1.142 B.142 — 1.143 B.143 —1.144 B.144 — 1.145 B.145 — 1.146 B.146 — 1.147 B.147 — 1.148 B.148 —1.149 B.149 — 1.150 B.150 — 1.151 B.151 — 1.152 B.152 — 1.153 B.153 —1.154 B.154 — 1.155 B.155 — 1.156 B.156 — 1.157 B.157 — 1.158 B.158 —1.159 B.159 — 1.160 B.160 — 1.161 B.161 — 1.162 B.162 — 1.163 B.163 —1.164 B.164 — 1.165 B.165 — 1.166 B.166 — 1.167 B.167 — 1.168 B.168 —1.169 B.169 — 1.170 B.170 — 1.171 B.171 — 1.172 B.172 — 1.173 B.173 —1.174 B.174 — 1.175 B.175 — 1.176 B.176 — 1.177 B.177 — 1.178 B.178 —1.179 B.179 — 1.180 B.180 — 1.181 B.181 — 1.182 B.182 — 1.183 B.183 —1.184 B.184 — 1.185 B.185 — 1.186 B.186 — 1.187 B.187 — 1.188 B.188 —1.189 B.189 — 1.190 B.190 1.191 B.191 1.192 B.192 1.193 B.193 1.194B.194 1.195 B.195 1.196 B.196 1.197 B.1 C.1 1.198 B.2 C.1 1.199 B.3 C.11.200 B.4 C.1 1.201 B.5 C.1 1.202 B.6 C.1 1.203 B.7 C.1 1.204 B.8 C.11.205 B.9 C.1 1.206 B.10 C.1 1.207 B.11 C.1 1.208 B.12 C.1 1.209 B.13C.1 1.210 B.14 C.1 1.211 B.15 C.1 1.212 B.16 C.1 1.213 B.17 C.1 1.214B.18 C.1 1.215 B.19 C.1 1.216 B.20 C.1 1.217 B.21 C.1 1.218 B.22 C.11.219 B.23 C.1 1.220 B.24 C.1 1.221 B.25 C.1 1.222 B.26 C.1 1.223 B.27C.1 1.224 B.28 C.1 1.225 B.29 C.1 1.226 B.30 C.1 1.227 B.31 C.1 1.228B.32 C.1 1.229 B.33 C.1 1.230 B.34 C.1 1.231 B.35 C.1 1.232 B.36 C.11.233 B.37 C.1 1.234 B.38 C.1 1.235 B.39 C.1 1.236 B.40 C.1 1.237 B.41C.1 1.238 B.42 C.1 1.239 B.43 C.1 1.240 B.44 C.1 1.241 B.45 C.1 1.242B.46 C.1 1.243 B.47 C.1 1.244 B.48 C.1 1.245 B.49 C.1 1.246 B.50 C.11.247 B.51 C.1 1.248 B.52 C.1 1.249 B.53 C.1 1.250 B.54 C.1 1.251 B.55C.1 1.252 B.56 C.1 1.253 B.57 C.1 1.254 B.58. C.1 1.255 B.59 C.1 1.256B.60 C.1 1.257 B.61 C.1 1.258 B.62 C.1 1.259 B.63 C.1 1.260 B.64 C.11.261 B.65 C.1 1.262 B.66 C.1 1.263 B.67 C.1 1.264 B.68 C.1 1.265 B.69C.1 1.266 B.70 C.1 1.267 B.71 C.1 1.268 B.72 C.1 1.269 B.73 C.1 1.270B.74 C.1 1.271 B.75 C.1 1.272 B.76 C.1 1.273 B.77 C.1 1.274 B.78 C.11.275 B.79 C.1 1.276 B.80 C.1 1.277 B.81 C.1 1.278 B.82 C.1 1.279 B.83C.1 1.280 B.84 C.1 1.281 B.85 C.1 1.282 B.86 C.1 1.283 B.87 C.1 1.284B.88 C.1 1.285 B.89 C.1 1.286 B.90 C.1 1.287 B.91 C.1 1.288 B.92 C.11.289 B.93 C.1 1.290 B.94 C.1 1.291 B.95 C.1 1.292 B.96 C.1 1.293 B.97C.1 1.294 B.98 C.1 1.295 B.99 C.1 1.296 B.100 C.1 1.297 B.101 C.1 1.298B.102 C.1 1.299 B.103 C.1 1.300 B.104 C.1 1.301 B.105 C.1 1.302 B.106C.1 1.303 B.107 C.1 1.304 B.108 C.1 1.305 B.109 C.1 1.306 B.110 C.11.307 B.111 C.1 1.308 B.112 C.1 1.309 B.113 C.1 1.310 B.114 C.1 1.311B.115 C.1 1.312 B.116 C.1 1.313 B.117 C.1 1.314 B.118 C.1 1.315 B.119C.1 1.316 B.120 C.1 1.317 B.121 C.1 1.318 B.122 C.1 1.319 B.123 C.11.320 B.124 C.1 1.321 B.125 C.1 1.322 B.126 C.1 1.323 B.127 C.1 1.324B.128 C.1 1.325 B.129 C.1 1.326 B.130 C.1 1.327 B.131 C.1 1.328 B.132C.1 1.329 B.133 C.1 1.330 B.134 C.1 1.331 B.135 C.1 1.332 B.136 C.11.333 B.137 C.1 1.334 B.138 C.1 1.335 B.139 C.1 1.336 B.140 C.1 1.337B.141 C.1 1.338 B.142 C.1 1.339 B.143 C.1 1.340 B.144 C.1 1.341 B.145C.1 1.342 B.146 C.1 1.343 B.147 C.1 1.344 B.148 C.1 1.345 B.149 C.11.346 B.150 C.1 1.347 B.151 C.1 1.348 B.152 C.1 1.349 B.153 C.1 1.350B.154 C.1 1.351 B.155 C.1 1.352 B.156 C.1 1.353 B.157 C.1 1.354 B.158C.1 1.355 B.159 C.1 1.356 B.160 C.1 1.357 B.161 C.1 1.358 B.162 C.11.359 B.163 C.1 1.360 B.164 C.1 1.361 B.165 C.1 1.362 B.166 C.1 1.363B.167 C.1 1.364 B.168 C.1 1.365 B.169 C.1 1.366 B.170 C.1 1.367 B.171C.1 1.368 B.172 C.1 1.369 B.173 C.1 1.370 B.174 C.1 1.371 B.175 C.11.372 B.176 C.1 1.373 B.177 C.1 1.374 B.178 C.1 1.375 B.179 C.1 1.376B.180 C.1 1.377 B.181 C.1 1.378 B.182 C.1 1.379 B.183 C.1 1.380 B.184C.1 1.381 B.185 C.1 1.382 B.186 C.1 1.383 B.187 C.1 1.384 B.188 C.11.385 B.189 C.1 1.386 B.190 C.1 1.387 B.191 C.1 1.388 B.192 C.1 1.389B.193 C.1 1.390 B.194 C.1 1.391 B.195 C.1 1.392 B.196 C.1 1.393 B.1 C.21.394 B.2 C.2 1.395 B.3 C.2 1.396 B.4 C.2 1.397 B.5 C.2 1.398 B.6 C.21.399 B.7 C.2 1.400 B.8 C.2 1.401 B.9 C.2 1.402 B.10 C.2 1.403 B.11 C.21.404 B.12 C.2 1.405 B.13 C.2 1.406 B.14 C.2 1.407 B.15 C.2 1.408 B.16C.2 1.409 B.17 C.2 1.410 B.18 C.2 1.411 B.19 C.2 1.412 B.20 C.2 1.413B.21 C.2 1.414 B.22 C.2 1.415 B.23 C.2 1.416 B.24 C.2 1.417 B.25 C.21.418 B.26 C.2 1.419 B.27 C.2 1.420 B.28 C.2 1.421 B.29 C.2 1.422 B.30C.2 1.423 B.31 C.2 1.424 B.32 C.2 1.425 B.33 C.2 1.426 B.34 C.2 1.427B.35 C.2 1.428 B.36 C.2 1.429 B.37 C.2 1.430 B.38 C.2 1.431 B.39 C.21.432 B.40 C.2 1.433 B.41 C.2 1.434 B.42 C.2 1.435 B.43 C.2 1.436 B.44C.2 1.437 B.45 C.2 1.438 B.46 C.2 1.439 B.47 C.2 1.440 B.48 C.2 1.441B.49 C.2 1.442 B.50 C.2 1.443 B.51 C.2 1.444 B.52 C.2 1.445 B.53 C.21.446 B.54 C.2 1.447 B.55 C.2 1.448 B.56 C.2 1.449 B.57 C.2 1.450 B.58.C.2 1.451 B.59 C.2 1.452 B.60 C.2 1.453 B.61 C.2 1.454 B.62 C.2 1.455B.63 C.2 1.456 B.64 C.2 1.457 B.65 C.2 1.458 B.66 C.2 1.459 B.67 C.21.460 B.68 C.2 1.461 B.69 C.2 1.462 B.70 C.2 1.463 B.71 C.2 1.464 B.72C.2 1.465 B.73 C.2 1.466 B.74 C.2 1.467 B.75 C.2 1.468 B.76 C.2 1.469B.77 C.2 1.470 B.78 C.2 1.471 B.79 C.2 1.472 B.80 C.2 1.473 B.81 C.21.474 B.82 C.2 1.475 B.83 C.2 1.476 B.84 C.2 1.477 B.85 C.2 1.478 B.86C.2 1.479 B.87 C.2 1.480 B.88 C.2 1.481 B.89 C.2 1.482 B.90 C.2 1.483B.91 C.2 1.484 B.92 C.2 1.485 B.93 C.2 1.486 B.94 C.2 1.487 B.95 C.21.488 B.96 C.2 1.489 B.97 C.2 1.490 B.98 C.2 1.491 B.99 C.2 1.492 B.100C.2 1.493 B.101 C.2 1.494 B.102 C.2 1.495 B.103 C.2 1.496 B.104 C.21.497 B.105 C.2 1.498 B.106 C.2 1.499 B.107 C.2 1.500 B.108 C.2 1.501B.109 C.2 1.502 B.110 C.2 1.503 B.111 C.2 1.504 B.112 C.2 1.505 B.113C.2 1.506 B.114 C.2 1.507 B.115 C.2 1.508 B.116 C.2 1.509 B.117 C.21.510 B.118 C.2 1.511 B.119 C.2 1.512 B.120 C.2 1.513 B.121 C.2 1.514B.122 C.2 1.515 B.123 C.2 1.516 B.124 C.2 1.517 B.125 C.2 1.518 B.126C.2 1.519 B.127 C.2 1.520 B.128 C.2 1.521 B.129 C.2 1.522 B.130 C.21.523 B.131 C.2 1.524 B.132 C.2 1.525 B.133 C.2 1.526 B.134 C.2 1.527B.135 C.2 1.528 B.136 C.2 1.529 B.137 C.2 1.530 B.138 C.2 1.531 B.139C.2 1.532 B.140 C.2 1.533 B.141 C.2 1.534 B.142 C.2 1.535 B.143 C.21.536 B.144 C.2 1.537 B.145 C.2 1.538 B.146 C.2 1.539 B.147 C.2 1.540B.148 C.2 1.541 B.149 C.2 1.542 B.150 C.2 1.543 B.151 C.2 1.544 B.152C.2 1.545 B.153 C.2 1.546 B.154 C.2 1.547 B.155 C.2 1.548 B.156 C.21.549 B.157 C.2 1.550 B.158 C.2 1.551 B.159 C.2 1.552 B.160 C.2 1.553B.161 C.2 1.554 B.162 C.2 1.555 B.163 C.2 1.556 B.164 C.2 1.557 B.165C.2 1.558 B.166 C.2 1.559 B.167 C.2 1.560 B.168 C.2 1.561 B.169 C.21.562 B.170 C.2 1.563 B.171 C.2 1.564 B.172 C.2 1.565 B.173 C.2 1.566B.174 C.2 1.567 B.175 C.2 1.568 B.176 C.2 1.569 B.177 C.2 1.570 B.178C.2 1.571 B.179 C.2 1.572 B.180 C.2 1.573 B.181 C.2 1.574 B.182 C.21.575 B.183 C.2 1.576 B.184 C.2 1.577 B.185 C.2 1.578 B.186 C.2 1.579B.187 C.2 1.580 B.188 C.2 1.581 B.189 C.2 1.582 B.190 C.2 1.583 B.191C.2 1.584 B.192 C.2 1.585 B.193 C.2 1.586 B.194 C.2 1.587 B.195 C.21.588 B.196 C.2 1.589 B.1 C.3 1.590 B.2 C.3 1.591 B.3 C.3 1.592 B.4 C.31.593 B.5 C.3 1.594 B.6 C.3 1.595 B.7 C.3 1.596 B.8 C.3 1.597 B.9 C.31.598 B.10 C.3 1.599 B.11 C.3 1.600 B.12 C.3 1.601 B.13 C.3 1.602 B.14C.3 1.603 B.15 C.3 1.604 B.16 C.3 1.605 B.17 C.3 1.606 B.18 C.3 1.607B.19 C.3 1.608 B.20 C.3 1.609 B.21 C.3 1.610 B.22 C.3 1.611 B.23 C.31.612 B.24 C.3 1.613 B.25 C.3 1.614 B.26 C.3 1.615 B.27 C.3 1.616 B.28C.3 1.617 B.29 C.3 1.618 B.30 C.3 1.619 B.31 C.3 1.620 B.32 C.3 1.621B.33 C.3 1.622 B.34 C.3 1.623 B.35 C.3 1.624 B.36 C.3 1.625 B.37 C.31.626 B.38 C.3 1.627 B.39 C.3 1.628 B.40 C.3 1.629 B.41 C.3 1.630 B.42C.3 1.631 B.43 C.3 1.632 B.44 C.3 1.633 B.45 C.3 1.634 B.46 C.3 1.635B.47 C.3 1.636 B.48 C.3 1.637 B.49 C.3 1.638 B.50 C.3 1.639 B.51 C.31.640 B.52 C.3 1.641 B.53 C.3 1.642 B.54 C.3 1.643 B.55 C.3 1.644 B.56C.3 1.645 B.57 C.3 1.646 B.58. C.3 1.647 B.59 C.3 1.648 B.60 C.3 1.649B.61 C.3 1.650 B.62 C.3 1.651 B.63 C.3 1.652 B.64 C.3 1.653 B.65 C.31.654 B.66 C.3 1.655 B.67 C.3 1.656 B.68 C.3 1.657 B.69 C.3 1.658 B.70C.3 1.659 B.71 C.3 1.660 B.72 C.3 1.661 B.73 C.3 1.662 B.74 C.3 1.663B.75 C.3 1.664 B.76 C.3 1.665 B.77 C.3 1.666 B.78 C.3 1.667 B.79 C.31.668 B.80 C.3 1.669 B.81 C.3 1.670 B.82 C.3 1.671 B.83 C.3 1.672 B.84C.3 1.673 B.85 C.3 1.674 B.86 C.3 1.675 B.87 C.3 1.676 B.88 C.3 1.677B.89 C.3 1.678 B.90 C.3 1.679 B.91 C.3 1.680 B.92 C.3 1.681 B.93 C.31.682 B.94 C.3 1.683 B.95 C.3 1.684 B.96 C.3 1.685 B.97 C.3 1.686 B.98C.3 1.687 B.99 C.3 1.688 B.100 C.3 1.689 B.101 C.3 1.690 B.102 C.3 1.691B.103 C.3 1.692 B.104 C.3 1.693 B.105 C.3 1.694 B.106 C.3 1.695 B.107C.3 1.696 B.108 C.3 1.697 B.109 C.3 1.698 B.110 C.3 1.699 B.111 C.31.700 B.112 C.3 1.701 B.113 C.3 1.702 B.114 C.3 1.703 B.115 C.3 1.704B.116 C.3 1.705 B.117 C.3 1.706 B.118 C.3 1.707 B.119 C.3 1.708 B.120C.3 1.709 B.121 C.3 1.710 B.122 C.3 1.711 B.123 C.3 1.712 B.124 C.31.713 B.125 C.3 1.714 B.126 C.3 1.715 B.127 C.3 1.716 B.128 C.3 1.717B.129 C.3 1.718 B.130 C.3 1.719 B.131 C.3 1.720 B.132 C.3 1.721 B.133C.3 1.722 B.134 C.3 1.723 B.135 C.3 1.724 B.136 C.3 1.725 B.137 C.31.726 B.138 C.3 1.727 B.139 C.3 1.728 B.140 C.3 1.729 B.141 C.3 1.730B.142 C.3 1.731 B.143 C.3 1.732 B.144 C.3 1.733 B.145 C.3 1.734 B.146C.3 1.735 B.147 C.3 1.736 B.148 C.3 1.737 B.149 C.3 1.738 B.150 C.31.739 B.151 C.3 1.740 B.152 C.3 1.741 B.153 C.3 1.742 B.154 C.3 1.743B.155 C.3 1.744 B.156 C.3 1.745 B.157 C.3 1.746 B.158 C.3 1.747 B.159C.3 1.748 B.160 C.3 1.749 B.161 C.3 1.750 B.162 C.3 1.751 B.163 C.31.752 B.164 C.3 1.753 B.165 C.3 1.754 B.166 C.3 1.755 B.167 C.3 1.756B.168 C.3 1.757 B.169 C.3 1.758 B.170 C.3 1.759 B.171 C.3 1.760 B.172C.3 1.761 B.173 C.3 1.762 B.174 C.3 1.763 B.175 C.3 1.764 B.176 C.31.765 B.177 C.3 1.766 B.178 C.3 1.767 B.179 C.3 1.768 B.180 C.3 1.769B.181 C.3 1.770 B.182 C.3 1.771 B.183 C.3 1.772 B.184 C.3 1.773 B.185C.3 1.774 B.186 C.3 1.775 B.187 C.3 1.776 B.188 C.3 1.777 B.189 C.31.778 B.190 C.3 1.779 B.191 C.3 1.780 B.192 C.3 1.781 B.193 C.3 1.782B.194 C.3 1.783 B.195 C.3 1.784 B.196 C.3 1.785 B.1 C.4 1.786 B.2 C.41.787 B.3 C.4 1.788 B.4 C.4 1.789 B.5 C.4 1.790 B.6 C.4 1.791 B.7 C.41.792 B.8 C.4 1.793 B.9 C.4 1.794 B.10 C.4 1.795 B.11 C.4 1.796 B.12 C.41.797 B.13 C.4 1.798 B.14 C.4 1.799 B.15 C.4 1.800 B.16 C.4 1.801 B.17C.4 1.802 B.18 C.4 1.803 B.19 C.4 1.804 B.20 C.4 1.805 B.21 C.4 1.806B.22 C.4 1.807 B.23 C.4 1.808 B.24 C.4 1.809 B.25 C.4 1.810 B.26 C.41.811 B.27 C.4 1.812 B.28 C.4 1.813 B.29 C.4 1.814 B.30 C.4 1.815 B.31C.4 1.816 B.32 C.4 1.817 B.33 C.4 1.818 B.34 C.4 1.819 B.35 C.4 1.820B.36 C.4 1.821 B.37 C.4 1.822 B.38 C.4 1.823 B.39 C.4 1.824 B.40 C.41.825 B.41 C.4 1.826 B.42 C.4 1.827 B.43 C.4 1.828 B.44 C.4 1.829 B.45C.4 1.830 B.46 C.4 1.831 B.47 C.4 1.832 B.48 C.4 1.833 B.49 C.4 1.834B.50 C.4 1.835 B.51 C.4 1.836 B.52 C.4 1.837 B.53 C.4 1.838 B.54 C.41.839 B.55 C.4 1.840 B.56 C.4 1.841 B.57 C.4 1.842 B.58. C.4 1.843 B.59C.4 1.844 B.60 C.4 1.845 B.61 C.4 1.846 B.62 C.4 1.847 B.63 C.4 1.848B.64 C.4 1.849 B.65 C.4 1.850 B.66 C.4 1.851 B.67 C.4 1.852 B.68 C.41.853 B.69 C.4 1.854 B.70 C.4 1.855 B.71 C.4 1.856 B.72 C.4 1.857 B.73C.4 1.858 B.74 C.4 1.859 B.75 C.4 1.860 B.76 C.4 1.861 B.77 C.4 1.862B.78 C.4 1.863 B.79 C.4 1.864 B.80 C.4 1.865 B.81 C.4 1.866 B.82 C.41.867 B.83 C.4 1.868 B.84 C.4 1.869 B.85 C.4 1.870 B.86 C.4 1.871 B.87C.4 1.872 B.88 C.4 1.873 B.89 C.4 1.874 B.90 C.4 1.875 B.91 C.4 1.876B.92 C.4 1.877 B.93 C.4 1.878 B.94 C.4 1.879 B.95 C.4 1.880 B.96 C.41.881 B.97 C.4 1.882 B.98 C.4 1.883 B.99 C.4 1.884 B.100 C.4 1.885 B.101C.4 1.886 B.102 C.4 1.887 B.103 C.4 1.888 B.104 C.4 1.889 B.105 C.41.890 B.106 C.4 1.891 B.107 C.4 1.892 B.108 C.4 1.893 B.109 C.4 1.894B.110 C.4 1.895 B.111 C.4 1.896 B.112 C.4 1.897 B.113 C.4 1.898 B.114C.4 1.899 B.115 C.4 1.900 B.116 C.4 1.901 B.117 C.4 1.902 B.118 C.41.903 B.119 C.4 1.904 B.120 C.4 1.905 B.121 C.4 1.906 B.122 C.4 1.907B.123 C.4 1.908 B.124 C.4 1.909 B.125 C.4 1.910 B.126 C.4 1.911 B.127C.4 1.912 B.128 C.4 1.913 B.129 C.4 1.914 B.130 C.4 1.915 B.131 C.41.916 B.132 C.4 1.917 B.133 C.4 1.918 B.134 C.4 1.919 B.135 C.4 1.920B.136 C.4 1.921 B.137 C.4 1.922 B.138 C.4 1.923 B.139 C.4 1.924 B.140C.4 1.925 B.141 C.4 1.926 B.142 C.4 1.927 B.143 C.4 1.928 B.144 C.41.929 B.145 C.4 1.930 B.146 C.4 1.931 B.147 C.4 1.932 B.148 C.4 1.933B.149 C.4 1.934 B.150 C.4 1.935 B.151 C.4 1.936 B.152 C.4 1.937 B.153C.4 1.938 B.154 C.4 1.939 B.155 C.4 1.940 B.156 C.4 1.941 B.157 C.41.942 B.158 C.4 1.943 B.159 C.4 1.944 B.160 C.4 1.945 B.161 C.4 1.946B.162 C.4 1.947 B.163 C.4 1.948 B.164 C.4 1.949 B.165 C.4 1.950 B.166C.4 1.951 B.167 C.4 1.952 B.168 C.4 1.953 B.169 C.4 1.954 B.170 C.41.955 B.171 C.4 1.956 B.172 C.4 1.957 B.173 C.4 1.958 B.174 C.4 1.959B.175 C.4 1.960 B.176 C.4 1.961 B.177 C.4 1.962 B.178 C.4 1.963 B.179C.4 1.964 B.180 C.4 1.965 B.181 C.4 1.966 B.182 C.4 1.967 B.183 C.41.968 B.184 C.4 1.969 B.185 C.4 1.970 B.186 C.4 1.971 B.187 C.4 1.972B.188 C.4 1.973 B.189 C.4 1.974 B.190 C.4 1.975 B.191 C.4 1.976 B.192C.4 1.977 B.193 C.4 1.978 B.194 C.4 1.979 B.195 C.4 1.980 B.196 C.41.981 B.1 C.5 1.982 B.2 C.5 1.983 B.3 C.5 1.984 B.4 C.5 1.985 B.5 C.51.986 B.6 C.5 1.987 B.7 C.5 1.988 B.8 C.5 1.989 B.9 C.5 1.990 B.10 C.51.991 B.11 C.5 1.992 B.12 C.5 1.993 B.13 C.5 1.994 B.14 C.5 1.995 B.15C.5 1.996 B.16 C.5 1.997 B.17 C.5 1.998 B.18 C.5 1.999 B.19 C.5 1.1000B.20 C.5 1.1001 B.21 C.5 1.1002 B.22 C.5 1.1003 B.23 C.5 1.1004 B.24 C.51.1005 B.25 C.5 1.1006 B.26 C.5 1.1007 B.27 C.5 1.1008 B.28 C.5 1.1009B.29 C.5 1.1010 B.30 C.5 1.1011 B.31 C.5 1.1012 B.32 C.5 1.1013 B.33 C.51.1014 B.34 C.5 1.1015 B.35 C.5 1.1016 B.36 C.5 1.1017 B.37 C.5 1.1018B.38 C.5 1.1019 B.39 C.5 1.1020 B.40 C.5 1.1021 B.41 C.5 1.1022 B.42 C.51.1023 B.43 C.5 1.1024 B.44 C.5 1.1025 B.45 C.5 1.1026 B.46 C.5 1.1027B.47 C.5 1.1028 B.48 C.5 1.1029 B.49 C.5 1.1030 B.50 C.5 1.1031 B.51 C.51.1032 B.52 C.5 1.1033 B.53 C.5 1.1034 B.54 C.5 1.1035 B.55 C.5 1.1036B.56 C.5 1.1037 B.57 C.5 1.1038 B.58. C.5 1.1039 B.59 C.5 1.1040 B.60C.5 1.1041 B.61 C.5 1.1042 B.62 C.5 1.1043 B.63 C.5 1.1044 B.64 C.51.1045 B.65 C.5 1.1046 B.66 C.5 1.1047 B.67 C.5 1.1048 B.68 C.5 1.1049B.69 C.5 1.1050 B.70 C.5 1.1051 B.71 C.5 1.1052 B.72 C.5 1.1053 B.73 C.51.1054 B.74 C.5 1.1055 B.75 C.5 1.1056 B.76 C.5 1.1057 B.77 C.5 1.1058B.78 C.5 1.1059 B.79 C.5 1.1060 B.80 C.5 1.1061 B.81 C.5 1.1062 B.82 C.51.1063 B.83 C.5 1.1064 B.84 C.5 1.1065 B.85 C.5 1.1066 B.86 C.5 1.1067B.87 C.5 1.1068 B.88 C.5 1.1069 B.89 C.5 1.1070 B.90 C.5 1.1071 B.91 C.51.1072 B.92 C.5 1.1073 B.93 C.5 1.1074 B.94 C.5 1.1075 B.95 C.5 1.1076B.96 C.5 1.1077 B.97 C.5 1.1078 B.98 C.5 1.1079 B.99 C.5 1.1080 B.100C.5 1.1081 B.101 C.5 1.1082 B.102 C.5 1.1083 B.103 C.5 1.1084 B.104 C.51.1085 B.105 C.5 1.1086 B.106 C.5 1.1087 B.107 C.5 1.1088 B.108 C.51.1089 B.109 C.5 1.1090 B.110 C.5 1.1091 B.111 C.5 1.1092 B.112 C.51.1093 B.113 C.5 1.1094 B.114 C.5 1.1095 B.115 C.5 1.1096 B.116 C.51.1097 B.117 C.5 1.1098 B.118 C.5 1.1099 B.119 C.5 1.1100 B.120 C.51.1101 B.121 C.5 1.1102 B.122 C.5 1.1103 B.123 C.5 1.1104 B.124 C.51.1105 B.125 C.5 1.1106 B.126 C.5 1.1107 B.127 C.5 1.1108 B.128 C.51.1109 B.129 C.5 1.1110 B.130 C.5 1.1111 B.131 C.5 1.1112 B.132 C.51.1113 B.133 C.5 1.1114 B.134 C.5 1.1115 B.135 C.5 1.1116 B.136 C.51.1117 B.137 C.5 1.1118 B.138 C.5 1.1119 B.139 C.5 1.1120 B.140 C.51.1121 B.141 C.5 1.1122 B.142 C.5 1.1123 B.143 C.5 1.1124 B.144 C.51.1125 B.145 C.5 1.1126 B.146 C.5 1.1127 B.147 C.5 1.1128 B.148 C.51.1129 B.149 C.5 1.1130 B.150 C.5 1.1131 B.151 C.5 1.1132 B.152 C.51.1133 B.153 C.5 1.1134 B.154 C.5 1.1135 B.155 C.5 1.1136 B.156 C.51.1137 B.157 C.5 1.1138 B.158 C.5 1.1139 B.159 C.5 1.1140 B.160 C.51.1141 B.161 C.5 1.1142 B.162 C.5 1.1143 B.163 C.5 1.1144 B.164 C.51.1145 B.165 C.5 1.1146 B.166 C.5 1.1147 B.167 C.5 1.1148 B.168 C.51.1149 B.169 C.5 1.1150 B.170 C.5 1.1151 B.171 C.5 1.1152 B.172 C.51.1153 B.173 C.5 1.1154 B.174 C.5 1.1155 B.175 C.5 1.1156 B.176 C.51.1157 B.177 C.5 1.1158 B.178 C.5 1.1159 B.179 C.5 1.1160 B.180 C.51.1161 B.181 C.5 1.1162 B.182 C.5 1.1163 B.183 C.5 1.1164 B.184 C.51.1165 B.185 C.5 1.1166 B.186 C.5 1.1167 B.187 C.5 1.1168 B.188 C.51.1169 B.189 C.5 1.1170 B.190 C.5 1.1171 B.191 C.5 1.1172 B.192 C.51.1173 B.193 C.5 1.1174 B.194 C.5 1.1175 B.195 C.5 1.1176 B.196 C.51.1177 B.1 C.6 1.1178 B.2 C.6 1.1179 B.3 C.6 1.1180 B.4 C.6 1.1181 B.5C.6 1.1182 B.6 C.6 1.1183 B.7 C.6 1.1184 B.8 C.6 1.1185 B.9 C.6 1.1186B.10 C.6 1.1187 B.11 C.6 1.1188 B.12 C.6 1.1189 B.13 C.6 1.1190 B.14 C.61.1191 B.15 C.6 1.1192 B.16 C.6 1.1193 B.17 C.6 1.1194 B.18 C.6 1.1195B.19 C.6 1.1196 B.20 C.6 1.1197 B.21 C.6 1.1198 B.22 C.6 1.1199 B.23 C.61.1200 B.24 C.6 1.1201 B.25 C.6 1.1202 B.26 C.6 1.1203 B.27 C.6 1.1204B.28 C.6 1.1205 B.29 C.6 1.1206 B.30 C.6 1.1207 B.31 C.6 1.1208 B.32 C.61.1209 B.33 C.6 1.1210 B.34 C.6 1.1211 B.35 C.6 1.1212 B.36 C.6 1.1213B.37 C.6 1.1214 B.38 C.6 1.1215 B.39 C.6 1.1216 B.40 C.6 1.1217 B.41 C.61.1218 B.42 C.6 1.1219 B.43 C.6 1.1220 B.44 C.6 1.1221 B.45 C.6 1.1222B.46 C.6 1.1223 B.47 C.6 1.1224 B.48 C.6 1.1225 B.49 C.6 1.1226 B.50 C.61.1227 B.51 C.6 1.1228 B.52 C.6 1.1229 B.53 C.6 1.1230 B.54 C.6 1.1231B.55 C.6 1.1232 B.56 C.6 1.1233 B.57 C.6 1.1234 B.58. C.6 1.1235 B.59C.6 1.1236 B.60 C.6 1.1237 B.61 C.6 1.1238 B.62 C.6 1.1239 B.63 C.61.1240 B.64 C.6 1.1241 B.65 C.6 1.1242 B.66 C.6 1.1243 B.67 C.6 1.1244B.68 C.6 1.1245 B.69 C.6 1.1246 B.70 C.6 1.1247 B.71 C.6 1.1248 B.72 C.61.1249 B.73 C.6 1.1250 B.74 C.6 1.1251 B.75 C.6 1.1252 B.76 C.6 1.1253B.77 C.6 1.1254 B.78 C.6 1.1255 B.79 C.6 1.1256 B.80 C.6 1.1257 B.81 C.61.1258 B.82 C.6 1.1259 B.83 C.6 1.1260 B.84 C.6 1.1261 B.85 C.6 1.1262B.86 C.6 1.1263 B.87 C.6 1.1264 B.88 C.6 1.1265 B.89 C.6 1.1266 B.90 C.61.1267 B.91 C.6 1.1268 B.92 C.6 1.1269 B.93 C.6 1.1270 B.94 C.6 1.1271B.95 C.6 1.1272 B.96 C.6 1.1273 B.97 C.6 1.1274 B.98 C.6 1.1275 B.99 C.61.1276 B.100 C.6 1.1277 B.101 C.6 1.1278 B.102 C.6 1.1279 B.103 C.61.1280 B.104 C.6 1.1281 B.105 C.6 1.1282 B.106 C.6 1.1283 B.107 C.61.1284 B.108 C.6 1.1285 B.109 C.6 1.1286 B.110 C.6 1.1287 B.111 C.61.1288 B.112 C.6 1.1289 B.113 C.6 1.1290 B.114 C.6 1.1291 B.115 C.61.1292 B.116 C.6 1.1293 B.117 C.6 1.1294 B.118 C.6 1.1295 B.119 C.61.1296 B.120 C.6 1.1297 B.121 C.6 1.1298 B.122 C.6 1.1299 B.123 C.61.1300 B.124 C.6 1.1301 B.125 C.6 1.1302 B.126 C.6 1.1303 B.127 C.61.1304 B.128 C.6 1.1305 B.129 C.6 1.1306 B.130 C.6 1.1307 B.131 C.61.1308 B.132 C.6 1.1309 B.133 C.6 1.1310 B.134 C.6 1.1311 B.135 C.61.1312 B.136 C.6 1.1313 B.137 C.6 1.1314 B.138 C.6 1.1315 B.139 C.61.1316 B.140 C.6 1.1317 B.141 C.6 1.1318 B.142 C.6 1.1319 B.143 C.61.1320 B.144 C.6 1.1321 B.145 C.6 1.1322 B.146 C.6 1.1323 B.147 C.61.1324 B.148 C.6 1.1325 B.149 C.6 1.1326 B.150 C.6 1.1327 B.151 C.61.1328 B.152 C.6 1.1329 B.153 C.6 1.1330 B.154 C.6 1.1331 B.155 C.61.1332 B.156 C.6 1.1333 B.157 C.6 1.1334 B.158 C.6 1.1335 B.159 C.61.1336 B.160 C.6 1.1337 B.161 C.6 1.1338 B.162 C.6 1.1339 B.163 C.61.1340 B.164 C.6 1.1341 B.165 C.6 1.1342 B.166 C.6 1.1343 B.167 C.61.1344 B.168 C.6 1.1345 B.169 C.6 1.1346 B.170 C.6 1.1347 B.171 C.61.1348 B.172 C.6 1.1349 B.173 C.6 1.1350 B.174 C.6 1.1351 B.175 C.61.1352 B.176 C.6 1.1353 B.177 C.6 1.1354 B.178 C.6 1.1355 B.179 C.61.1356 B.180 C.6 1.1357 B.181 C.6 1.1358 B.182 C.6 1.1359 B.183 C.61.1360 B.184 C.6 1.1361 B.185 C.6 1.1362 B.186 C.6 1.1363 B.187 C.61.1364 B.188 C.6 1.1365 B.189 C.6 1.1366 B.190 C.6 1.1367 B.191 C.61.1368 B.192 C.6 1.1369 B.193 C.6 1.1370 B.194 C.6 1.1371 B.195 C.61.1372 B.196 C.6 1.1373 B.1 C.7 1.1374 B.2 C.7 1.1375 B.3 C.7 1.1376 B.4C.7 1.1377 B.5 C.7 1.1378 B.6 C.7 1.1379 B.7 C.7 1.1380 B.8 C.7 1.1381B.9 C.7 1.1382 B.10 C.7 1.1383 B.11 C.7 1.1384 B.12 C.7 1.1385 B.13 C.71.1386 B.14 C.7 1.1387 B.15 C.7 1.1388 B.16 C.7 1.1389 B.17 C.7 1.1390B.18 C.7 1.1391 B.19 C.7 1.1392 B.20 C.7 1.1393 B.21 C.7 1.1394 B.22 C.71.1395 B.23 C.7 1.1396 B.24 C.7 1.1397 B.25 C.7 1.1398 B.26 C.7 1.1399B.27 C.7 1.1400 B.28 C.7 1.1401 B.29 C.7 1.1402 B.30 C.7 1.1403 B.31 C.71.1404 B.32 C.7 1.1405 B.33 C.7 1.1406 B.34 C.7 1.1407 B.35 C.7 1.1408B.36 C.7 1.1409 B.37 C.7 1.1410 B.38 C.7 1.1411 B.39 C.7 1.1412 B.40 C.71.1413 B.41 C.7 1.1414 B.42 C.7 1.1415 B.43 C.7 1.1416 B.44 C.7 1.1417B.45 C.7 1.1418 B.46 C.7 1.1419 B.47 C.7 1.1420 B.48 C.7 1.1421 B.49 C.71.1422 B.50 C.7 1.1423 B.51 C.7 1.1424 B.52 C.7 1.1425 B.53 C.7 1.1426B.54 C.7 1.1427 B.55 C.7 1.1428 B.56 C.7 1.1429 B.57 C.7 1.1430 B.58.C.7 1.1431 B.59 C.7 1.1432 B.60 C.7 1.1433 B.61 C.7 1.1434 B.62 C.71.1435 B.63 C.7 1.1436 B.64 C.7 1.1437 B.65 C.7 1.1438 B.66 C.7 1.1439B.67 C.7 1.1440 B.68 C.7 1.1441 B.69 C.7 1.1442 B.70 C.7 1.1443 B.71 C.71.1444 B.72 C.7 1.1445 B.73 C.7 1.1446 B.74 C.7 1.1447 B.75 C.7 1.1448B.76 C.7 1.1449 B.77 C.7 1.1450 B.78 C.7 1.1451 B.79 C.7 1.1452 B.80 C.71.1453 B.81 C.7 1.1454 B.82 C.7 1.1455 B.83 C.7 1.1456 B.84 C.7 1.1457B.85 C.7 1.1458 B.86 C.7 1.1459 B.87 C.7 1.1460 B.88 C.7 1.1461 B.89 C.71.1462 B.90 C.7 1.1463 B.91 C.7 1.1464 B.92 C.7 1.1465 B.93 C.7 1.1466B.94 C.7 1.1467 B.95 C.7 1.1468 B.96 C.7 1.1469 B.97 C.7 1.1470 B.98 C.71.1471 B.99 C.7 1.1472 B.100 C.7 1.1473 B.101 C.7 1.1474 B.102 C.71.1475 B.103 C.7 1.1476 B.104 C.7 1.1477 B.105 C.7 1.1478 B.106 C.71.1479 B.107 C.7 1.1480 B.108 C.7 1.1481 B.109 C.7 1.1482 B.110 C.71.1483 B.111 C.7 1.1484 B.112 C.7 1.1485 B.113 C.7 1.1486 B.114 C.71.1487 B.115 C.7 1.1488 B.116 C.7 1.1489 B.117 C.7 1.1490 B.118 C.71.1491 B.119 C.7 1.1492 B.120 C.7 1.1493 B.121 C.7 1.1494 B.122 C.71.1495 B.123 C.7 1.1496 B.124 C.7 1.1497 B.125 C.7 1.1498 B.126 C.71.1499 B.127 C.7 1.1500 B.128 C.7 1.1501 B.129 C.7 1.1502 B.130 C.71.1503 B.131 C.7 1.1504 B.132 C.7 1.1505 B.133 C.7 1.1506 B.134 C.71.1507 B.135 C.7 1.1508 B.136 C.7 1.1509 B.137 C.7 1.1510 B.138 C.71.1511 B.139 C.7 1.1512 B.140 C.7 1.1513 B.141 C.7 1.1514 B.142 C.71.1515 B.143 C.7 1.1516 B.144 C.7 1.1517 B.145 C.7 1.1518 B.146 C.71.1519 B.147 C.7 1.1520 B.148 C.7 1.1521 B.149 C.7 1.1522 B.150 C.71.1523 B.151 C.7 1.1524 B.152 C.7 1.1525 B.153 C.7 1.1526 B.154 C.71.1527 B.155 C.7 1.1528 B.156 C.7 1.1529 B.157 C.7 1.1530 B.158 C.71.1531 B.159 C.7 1.1532 B.160 C.7 1.1533 B.161 C.7 1.1534 B.162 C.71.1535 B.163 C.7 1.1536 B.164 C.7 1.1537 B.165 C.7 1.1538 B.166 C.71.1539 B.167 C.7 1.1540 B.168 C.7 1.1541 B.169 C.7 1.1542 B.170 C.71.1543 B.171 C.7 1.1544 B.172 C.7 1.1545 B.173 C.7 1.1546 B.174 C.71.1547 B.175 C.7 1.1548 B.176 C.7 1.1549 B.177 C.7 1.1550 B.178 C.71.1551 B.179 C.7 1.1552 B.180 C.7 1.1553 B.181 C.7 1.1554 B.182 C.71.1555 B.183 C.7 1.1556 B.184 C.7 1.1557 B.185 C.7 1.1558 B.186 C.71.1559 B.187 C.7 1.1560 B.188 C.7 1.1561 B.189 C.7 1.1562 B.190 C.71.1563 B.191 C.7 1.1564 B.192 C.7 1.1565 B.193 C.7 1.1566 B.194 C.71.1567 B.195 C.7 1.1568 B.196 C.7 1.1569 B.1 C.8 1.1570 B.2 C.8 1.1571B.3 C.8 1.1572 B.4 C.8 1.1573 B.5 C.8 1.1574 B.6 C.8 1.1575 B.7 C.81.1576 B.8 C.8 1.1577 B.9 C.8 1.1578 B.10 C.8 1.1579 B.11 C.8 1.1580B.12 C.8 1.1581 B.13 C.8 1.1582 B.14 C.8 1.1583 B.15 C.8 1.1584 B.16 C.81.1585 B.17 C.8 1.1586 B.18 C.8 1.1587 B.19 C.8 1.1588 B.20 C.8 1.1589B.21 C.8 1.1590 B.22 C.8 1.1591 B.23 C.8 1.1592 B.24 C.8 1.1593 B.25 C.81.1594 B.26 C.8 1.1595 B.27 C.8 1.1596 B.28 C.8 1.1597 B.29 C.8 1.1598B.30 C.8 1.1599 B.31 C.8 1.1600 B.32 C.8 1.1601 B.33 C.8 1.1602 B.34 C.81.1603 B.35 C.8 1.1604 B.36 C.8 1.1605 B.37 C.8 1.1606 B.38 C.8 1.1607B.39 C.8 1.1608 B.40 C.8 1.1609 B.41 C.8 1.1610 B.42 C.8 1.1611 B.43 C.81.1612 B.44 C.8 1.1613 B.45 C.8 1.1614 B.46 C.8 1.1615 B.47 C.8 1.1616B.48 C.8 1.1617 B.49 C.8 1.1618 B.50 C.8 1.1619 B.51 C.8 1.1620 B.52 C.81.1621 B.53 C.8 1.1622 B.54 C.8 1.1623 B.55 C.8 1.1624 B.56 C.8 1.1625B.57 C.8 1.1626 B.58. C.8 1.1627 B.59 C.8 1.1628 B.60 C.8 1.1629 B.61C.8 1.1630 B.62 C.8 1.1631 B.63 C.8 1.1632 B.64 C.8 1.1633 B.65 C.81.1634 B.66 C.8 1.1635 B.67 C.8 1.1636 B.68 C.8 1.1637 B.69 C.8 1.1638B.70 C.8 1.1639 B.71 C.8 1.1640 B.72 C.8 1.1641 B.73 C.8 1.1642 B.74 C.81.1643 B.75 C.8 1.1644 B.76 C.8 1.1645 B.77 C.8 1.1646 B.78 C.8 1.1647B.79 C.8 1.1648 B.80 C.8 1.1649 B.81 C.8 1.1650 B.82 C.8 1.1651 B.83 C.81.1652 B.84 C.8 1.1653 B.85 C.8 1.1654 B.86 C.8 1.1655 B.87 C.8 1.1656B.88 C.8 1.1657 B.89 C.8 1.1658 B.90 C.8 1.1659 B.91 C.8 1.1660 B.92 C.81.1661 B.93 C.8 1.1662 B.94 C.8 1.1663 B.95 C.8 1.1664 B.96 C.8 1.1665B.97 C.8 1.1666 B.98 C.8 1.1667 B.99 C.8 1.1668 B.100 C.8 1.1669 B.101C.8 1.1670 B.102 C.8 1.1671 B.103 C.8 1.1672 B.104 C.8 1.1673 B.105 C.81.1674 B.106 C.8 1.1675 B.107 C.8 1.1676 B.108 C.8 1.1677 B.109 C.81.1678 B.110 C.8 1.1679 B.111 C.8 1.1680 B.112 C.8 1.1681 B.113 C.81.1682 B.114 C.8 1.1683 B.115 C.8 1.1684 B.116 C.8 1.1685 B.117 C.81.1686 B.118 C.8 1.1687 B.119 C.8 1.1688 B.120 C.8 1.1689 B.121 C.81.1690 B.122 C.8 1.1691 B.123 C.8 1.1692 B.124 C.8 1.1693 B.125 C.81.1694 B.126 C.8 1.1695 B.127 C.8 1.1696 B.128 C.8 1.1697 B.129 C.81.1698 B.130 C.8 1.1699 B.131 C.8 1.1700 B.132 C.8 1.1701 B.133 C.81.1702 B.134 C.8 1.1703 B.135 C.8 1.1704 B.136 C.8 1.1705 B.137 C.81.1706 B.138 C.8 1.1707 B.139 C.8 1.1708 B.140 C.8 1.1709 B.141 C.81.1710 B.142 C.8 1.1711 B.143 C.8 1.1712 B.144 C.8 1.1713 B.145 C.81.1714 B.146 C.8 1.1715 B.147 C.8 1.1716 B.148 C.8 1.1717 B.149 C.81.1718 B.150 C.8 1.1719 B.151 C.8 1.1720 B.152 C.8 1.1721 B.153 C.81.1722 B.154 C.8 1.1723 B.155 C.8 1.1724 B.156 C.8 1.1725 B.157 C.81.1726 B.158 C.8 1.1727 B.159 C.8 1.1728 B.160 C.8 1.1729 B.161 C.81.1730 B.162 C.8 1.1731 B.163 C.8 1.1732 B.164 C.8 1.1733 B.165 C.81.1734 B.166 C.8 1.1735 B.167 C.8 1.1736 B.168 C.8 1.1737 B.169 C.81.1738 B.170 C.8 1.1739 B.171 C.8 1.1740 B.172 C.8 1.1741 B.173 C.81.1742 B.174 C.8 1.1743 B.175 C.8 1.1744 B.176 C.8 1.1745 B.177 C.81.1746 B.178 C.8 1.1747 B.179 C.8 1.1748 B.180 C.8 1.1749 B.181 C.81.1750 B.182 C.8 1.1751 B.183 C.8 1.1752 B.184 C.8 1.1753 B.185 C.81.1754 B.186 C.8 1.1755 B.187 C.8 1.1756 B.188 C.8 1.1757 B.189 C.81.1758 B.190 C.8 1.1759 B.191 C.8 1.1760 B.192 C.8 1.1761 B.193 C.81.1762 B.194 C.8 1.1763 B.195 C.8 1.1764 B.196 C.8 1.1765 B.1 C.9 1.1766B.2 C.9 1.1767 B.3 C.9 1.1768 B.4 C.9 1.1769 B.5 C.9 1.1770 B.6 C.91.1771 B.7 C.9 1.1772 B.8 C.9 1.1773 B.9 C.9 1.1774 B.10 C.9 1.1775 B.11C.9 1.1776 B.12 C.9 1.1777 B.13 C.9 1.1778 B.14 C.9 1.1779 B.15 C.91.1780 B.16 C.9 1.1781 B.17 C.9 1.1782 B.18 C.9 1.1783 B.19 C.9 1.1784B.20 C.9 1.1785 B.21 C.9 1.1786 B.22 C.9 1.1787 B.23 C.9 1.1788 B.24 C.91.1789 B.25 C.9 1.1790 B.26 C.9 1.1791 B.27 C.9 1.1792 B.28 C.9 1.1793B.29 C.9 1.1794 B.30 C.9 1.1795 B.31 C.9 1.1796 B.32 C.9 1.1797 B.33 C.91.1798 B.34 C.9 1.1799 B.35 C.9 1.1800 B.36 C.9 1.1801 B.37 C.9 1.1802B.38 C.9 1.1803 B.39 C.9 1.1804 B.40 C.9 1.1805 B.41 C.9 1.1806 B.42 C.91.1807 B.43 C.9 1.1808 B.44 C.9 1.1809 B.45 C.9 1.1810 B.46 C.9 1.1811B.47 C.9 1.1812 B.48 C.9 1.1813 B.49 C.9 1.1814 B.50 C.9 1.1815 B.51 C.91.1816 B.52 C.9 1.1817 B.53 C.9 1.1818 B.54 C.9 1.1819 B.55 C.9 1.1820B.56 C.9 1.1821 B.57 C.9 1.1822 B.58. C.9 1.1823 B.59 C.9 1.1824 B.60C.9 1.1825 B.61 C.9 1.1826 B.62 C.9 1.1827 B.63 C.9 1.1828 B.64 C.91.1829 B.65 C.9 1.1830 B.66 C.9 1.1831 B.67 C.9 1.1832 B.68 C.9 1.1833B.69 C.9 1.1834 B.70 C.9 1.1835 B.71 C.9 1.1836 B.72 C.9 1.1837 B.73 C.91.1838 B.74 C.9 1.1839 B.75 C.9 1.1840 B.76 C.9 1.1841 B.77 C.9 1.1842B.78 C.9 1.1843 B.79 C.9 1.1844 B.80 C.9 1.1845 B.81 C.9 1.1846 B.82 C.91.1847 B.83 C.9 1.1848 B.84 C.9 1.1849 B.85 C.9 1.1850 B.86 C.9 1.1851B.87 C.9 1.1852 B.88 C.9 1.1853 B.89 C.9 1.1854 B.90 C.9 1.1855 B.91 C.91.1856 B.92 C.9 1.1857 B.93 C.9 1.1858 B.94 C.9 1.1859 B.95 C.9 1.1860B.96 C.9 1.1861 B.97 C.9 1.1862 B.98 C.9 1.1863 B.99 C.9 1.1864 B.100C.9 1.1865 B.101 C.9 1.1866 B.102 C.9 1.1867 B.103 C.9 1.1868 B.104 C.91.1869 B.105 C.9 1.1870 B.106 C.9 1.1871 B.107 C.9 1.1872 B.108 C.91.1873 B.109 C.9 1.1874 B.110 C.9 1.1875 B.111 C.9 1.1876 B.112 C.91.1877 B.113 C.9 1.1878 B.114 C.9 1.1879 B.115 C.9 1.1880 B.116 C.91.1881 B.117 C.9 1.1882 B.118 C.9 1.1883 B.119 C.9 1.1884 B.120 C.91.1885 B.121 C.9 1.1886 B.122 C.9 1.1887 B.123 C.9 1.1888 B.124 C.91.1889 B.125 C.9 1.1890 B.126 C.9 1.1891 B.127 C.9 1.1892 B.128 C.91.1893 B.129 C.9 1.1894 B.130 C.9 1.1895 B.131 C.9 1.1896 B.132 C.91.1897 B.133 C.9 1.1898 B.134 C.9 1.1899 B.135 C.9 1.1900 B.136 C.91.1901 B.137 C.9 1.1902 B.138 C.9 1.1903 B.139 C.9 1.1904 B.140 C.91.1905 B.141 C.9 1.1906 B.142 C.9 1.1907 B.143 C.9 1.1908 B.144 C.91.1909 B.145 C.9 1.1910 B.146 C.9 1.1911 B.147 C.9 1.1912 B.148 C.91.1913 B.149 C.9 1.1914 B.150 C.9 1.1915 B.151 C.9 1.1916 B.152 C.91.1917 B.153 C.9 1.1918 B.154 C.9 1.1919 B.155 C.9 1.1920 B.156 C.91.1921 B.157 C.9 1.1922 B.158 C.9 1.1923 B.159 C.9 1.1924 B.160 C.91.1925 B.161 C.9 1.1926 B.162 C.9 1.1927 B.163 C.9 1.1928 B.164 C.91.1929 B.165 C.9 1.1930 B.166 C.9 1.1931 B.167 C.9 1.1932 B.168 C.91.1933 B.169 C.9 1.1934 B.170 C.9 1.1935 B.171 C.9 1.1936 B.172 C.91.1937 B.173 C.9 1.1938 B.174 C.9 1.1939 B.175 C.9 1.1940 B.176 C.91.1941 B.177 C.9 1.1942 B.178 C.9 1.1943 B.179 C.9 1.1944 B.180 C.91.1945 B.181 C.9 1.1946 B.182 C.9 1.1947 B.183 C.9 1.1948 B.184 C.91.1949 B.185 C.9 1.1950 B.186 C.9 1.1951 B.187 C.9 1.1952 B.188 C.91.1953 B.189 C.9 1.1954 B.190 C.9 1.1955 B.191 C.9 1.1956 B.192 C.91.1957 B.193 C.9 1.1958 B.194 C.9 1.1959 B.195 C.9 1.1960 B.196 C.91.1961 B.1 C.10 1.1962 B.2 C.10 1.1963 B.3 C.10 1.1964 B.4 C.10 1.1965B.5 C.10 1.1966 B.6 C.10 1.1967 B.7 C.10 1.1968 B.8 C.10 1.1969 B.9 C.101.1970 B.10 C.10 1.1971 B.11 C.10 1.1972 B.12 C.10 1.1973 B.13 C.101.1974 B.14 C.10 1.1975 B.15 C.10 1.1976 B.16 C.10 1.1977 B.17 C.101.1978 B.18 C.10 1.1979 B.19 C.10 1.1980 B.20 C.10 1.1981 B.21 C.101.1982 B.22 C.10 1.1983 B.23 C.10 1.1984 B.24 C.10 1.1985 B.25 C.101.1986 B.26 C.10 1.1987 B.27 C.10 1.1988 B.28 C.10 1.1989 B.29 C.101.1990 B.30 C.10 1.1991 B.31 C.10 1.1992 B.32 C.10 1.1993 B.33 C.101.1994 B.34 C.10 1.1995 B.35 C.10 1.1996 B.36 C.10 1.1997 B.37 C.101.1998 B.38 C.10 1.1999 B.39 C.10 1.2000 B.40 C.10 1.2001 B.41 C.101.2002 B.42 C.10 1.2003 B.43 C.10 1.2004 B.44 C.10 1.2005 B.45 C.101.2006 B.46 C.10 1.2007 B.47 C.10 1.2008 B.48 C.10 1.2009 B.49 C.101.2010 B.50 C.10 1.2011 B.51 C.10 1.2012 B.52 C.10 1.2013 B.53 C.101.2014 B.54 C.10 1.2015 B.55 C.10 1.2016 B.56 C.10 1.2017 B.57 C.101.2018 B.58. C.10 1.2019 B.59 C.10 1.2020 B.60 C.10 1.2021 B.61 C.101.2022 B.62 C.10 1.2023 B.63 C.10 1.2024 B.64 C.10 1.2025 B.65 C.101.2026 B.66 C.10 1.2027 B.67 C.10 1.2028 B.68 C.10 1.2029 B.69 C.101.2030 B.70 C.10 1.2031 B.71 C.10 1.2032 B.72 C.10 1.2033 B.73 C.101.2034 B.74 C.10 1.2035 B.75 C.10 1.2036 B.76 C.10 1.2037 B.77 C.101.2038 B.78 C.10 1.2039 B.79 C.10 1.2040 B.80 C.10 1.2041 B.81 C.101.2042 B.82 C.10 1.2043 B.83 C.10 1.2044 B.84 C.10 1.2045 B.85 C.101.2046 B.86 C.10 1.2047 B.87 C.10 1.2048 B.88 C.10 1.2049 B.89 C.101.2050 B.90 C.10 1.2051 B.91 C.10 1.2052 B.92 C.10 1.2053 B.93 C.101.2054 B.94 C.10 1.2055 B.95 C.10 1.2056 B.96 C.10 1.2057 B.97 C.101.2058 B.98 C.10 1.2059 B.99 C.10 1.2060 B.100 C.10 1.2061 B.101 C.101.2062 B.102 C.10 1.2063 B.103 C.10 1.2064 B.104 C.10 1.2065 B.105 C.101.2066 B.106 C.10 1.2067 B.107 C.10 1.2068 B.108 C.10 1.2069 B.109 C.101.2070 B.110 C.10 1.2071 B.111 C.10 1.2072 B.112 C.10 1.2073 B.113 C.101.2074 B.114 C.10 1.2075 B.115 C.10 1.2076 B.116 C.10 1.2077 B.117 C.101.2078 B.118 C.10 1.2079 B.119 C.10 1.2080 B.120 C.10 1.2081 B.121 C.101.2082 B.122 C.10 1.2083 B.123 C.10 1.2084 B.124 C.10 1.2085 B.125 C.101.2086 B.126 C.10 1.2087 B.127 C.10 1.2088 B.128 C.10 1.2089 B.129 C.101.2090 B.130 C.10 1.2091 B.131 C.10 1.2092 B.132 C.10 1.2093 B.133 C.101.2094 B.134 C.10 1.2095 B.135 C.10 1.2096 B.136 C.10 1.2097 B.137 C.101.2098 B.138 C.10 1.2099 B.139 C.10 1.2100 B.140 C.10 1.2101 B.141 C.101.2102 B.142 C.10 1.2103 B.143 C.10 1.2104 B.144 C.10 1.2105 B.145 C.101.2106 B.146 C.10 1.2107 B.147 C.10 1.2108 B.148 C.10 1.2109 B.149 C.101.2110 B.150 C.10 1.2111 B.151 C.10 1.2112 B.152 C.10 1.2113 B.153 C.101.2114 B.154 C.10 1.2115 B.155 C.10 1.2116 B.156 C.10 1.2117 B.157 C.101.2118 B.158 C.10 1.2119 B.159 C.10 1.2120 B.160 C.10 1.2121 B.161 C.101.2122 B.162 C.10 1.2123 B.163 C.10 1.2124 B.164 C.10 1.2125 B.165 C.101.2126 B.166 C.10 1.2127 B.167 C.10 1.2128 B.168 C.10 1.2129 B.169 C.101.2130 B.170 C.10 1.2131 B.171 C.10 1.2132 B.172 C.10 1.2133 B.173 C.101.2134 B.174 C.10 1.2135 B.175 C.10 1.2136 B.176 C.10 1.2137 B.177 C.101.2138 B.178 C.10 1.2139 B.179 C.10 1.2140 B.180 C.10 1.2141 B.181 C.101.2142 B.182 C.10 1.2143 B.183 C.10 1.2144 B.184 C.10 1.2145 B.185 C.101.2146 B.186 C.10 1.2147 B.187 C.10 1.2148 B.188 C.10 1.2149 B.189 C.101.2150 B.190 C.10 1.2151 B.191 C.10 1.2152 B.192 C.10 1.2153 B.193 C.101.2154 B.194 C.10 1.2155 B.195 C.10 1.2156 B.196 C.10 1.2157 B.1 C.111.2158 B.2 C.11 1.2159 B.3 C.11 1.2160 B.4 C.11 1.2161 B.5 C.11 1.2162B.6 C.11 1.2163 B.7 C.11 1.2164 B.8 C.11 1.2165 B.9 C.11 1.2166 B.10C.11 1.2167 B.11 C.11 1.2168 B.12 C.11 1.2169 B.13 C.11 1.2170 B.14 C.111.2171 B.15 C.11 1.2172 B.16 C.11 1.2173 B.17 C.11 1.2174 B.18 C.111.2175 B.19 C.11 1.2176 B.20 C.11 1.2177 B.21 C.11 1.2178 B.22 C.111.2179 B.23 C.11 1.2180 B.24 C.11 1.2181 B.25 C.11 1.2182 B.26 C.111.2183 B.27 C.11 1.2184 B.28 C.11 1.2185 B.29 C.11 1.2186 B.30 C.111.2187 B.31 C.11 1.2188 B.32 C.11 1.2189 B.33 C.11 1.2190 B.34 C.111.2191 B.35 C.11 1.2192 B.36 C.11 1.2193 B.37 C.11 1.2194 B.38 C.111.2195 B.39 C.11 1.2196 B.40 C.11 1.2197 B.41 C.11 1.2198 B.42 C.111.2199 B.43 C.11 1.2200 B.44 C.11 1.2201 B.45 C.11 1.2202 B.46 C.111.2203 B.47 C.11 1.2204 B.48 C.11 1.2205 B.49 C.11 1.2206 B.50 C.111.2207 B.51 C.11 1.2208 B.52 C.11 1.2209 B.53 C.11 1.2210 B.54 C.111.2211 B.55 C.11 1.2212 B.56 C.11 1.2213 B.57 C.11 1.2214 B.58. C.111.2215 B.59 C.11 1.2216 B.60 C.11 1.2217 B.61 C.11 1.2218 B.62 C.111.2219 B.63 C.11 1.2220 B.64 C.11 1.2221 B.65 C.11 1.2222 B.66 C.111.2223 B.67 C.11 1.2224 B.68 C.11 1.2225 B.69 C.11 1.2226 B.70 C.111.2227 B.71 C.11 1.2228 B.72 C.11 1.2229 B.73 C.11 1.2230 B.74 C.111.2231 B.75 C.11 1.2232 B.76 C.11 1.2233 B.77 C.11 1.2234 B.78 C.111.2235 B.79 C.11 1.2236 B.80 C.11 1.2237 B.81 C.11 1.2238 B.82 C.111.2239 B.83 C.11 1.2240 B.84 C.11 1.2241 B.85 C.11 1.2242 B.86 C.111.2243 B.87 C.11 1.2244 B.88 C.11 1.2245 B.89 C.11 1.2246 B.90 C.111.2247 B.91 C.11 1.2248 B.92 C.11 1.2249 B.93 C.11 1.2250 B.94 C.111.2251 B.95 C.11 1.2252 B.96 C.11 1.2253 B.97 C.11 1.2254 B.98 C.111.2255 B.99 C.11 1.2256 B.100 C.11 1.2257 B.101 C.11 1.2258 B.102 C.111.2259 B.103 C.11 1.2260 B.104 C.11 1.2261 B.105 C.11 1.2262 B.106 C.111.2263 B.107 C.11 1.2264 B.108 C.11 1.2265 B.109 C.11 1.2266 B.110 C.111.2267 B.111 C.11 1.2268 B.112 C.11 1.2269 B.113 C.11 1.2270 B.114 C.111.2271 B.115 C.11 1.2272 B.116 C.11 1.2273 B.117 C.11 1.2274 B.118 C.111.2275 B.119 C.11 1.2276 B.120 C.11 1.2277 B.121 C.11 1.2278 B.122 C.111.2279 B.123 C.11 1.2280 B.124 C.11 1.2281 B.125 C.11 1.2282 B.126 C.111.2283 B.127 C.11 1.2284 B.128 C.11 1.2285 B.129 C.11 1.2286 B.130 C.111.2287 B.131 C.11 1.2288 B.132 C.11 1.2289 B.133 C.11 1.2290 B.134 C.111.2291 B.135 C.11 1.2292 B.136 C.11 1.2293 B.137 C.11 1.2294 B.138 C.111.2295 B.139 C.11 1.2296 B.140 C.11 1.2297 B.141 C.11 1.2298 B.142 C.111.2299 B.143 C.11 1.2300 B.144 C.11 1.2301 B.145 C.11 1.2302 B.146 C.111.2303 B.147 C.11 1.2304 B.148 C.11 1.2305 B.149 C.11 1.2306 B.150 C.111.2307 B.151 C.11 1.2308 B.152 C.11 1.2309 B.153 C.11 1.2310 B.154 C.111.2311 B.155 C.11 1.2312 B.156 C.11 1.2313 B.157 C.11 1.2314 B.158 C.111.2315 B.159 C.11 1.2316 B.160 C.11 1.2317 B.161 C.11 1.2318 B.162 C.111.2319 B.163 C.11 1.2320 B.164 C.11 1.2321 B.165 C.11 1.2322 B.166 C.111.2323 B.167 C.11 1.2324 B.168 C.11 1.2325 B.169 C.11 1.2326 B.170 C.111.2327 B.171 C.11 1.2328 B.172 C.11 1.2329 B.173 C.11 1.2330 B.174 C.111.2331 B.175 C.11 1.2332 B.176 C.11 1.2333 B.177 C.11 1.2334 B.178 C.111.2335 B.179 C.11 1.2336 B.180 C.11 1.2337 B.181 C.11 1.2338 B.182 C.111.2339 B.183 C.11 1.2340 B.184 C.11 1.2341 B.185 C.11 1.2342 B.186 C.111.2343 B.187 C.11 1.2344 B.188 C.11 1.2345 B.189 C.11 1.2346 B.190 C.111.2347 B.191 C.11 1.2348 B.192 C.11 1.2349 B.193 C.11 1.2350 B.194 C.111.2351 B.195 C.11 1.2352 B.196 C.11 1.2353 B.1 C.12 1.2354 B.2 C.121.2355 B.3 C.12 1.2356 B.4 C.12 1.2357 B.5 C.12 1.2358 B.6 C.12 1.2359B.7 C.12 1.2360 B.8 C.12 1.2361 B.9 C.12 1.2362 B.10 C.12 1.2363 B.11C.12 1.2364 B.12 C.12 1.2365 B.13 C.12 1.2366 B.14 C.12 1.2367 B.15 C.121.2368 B.16 C.12 1.2369 B.17 C.12 1.2370 B.18 C.12 1.2371 B.19 C.121.2372 B.20 C.12 1.2373 B.21 C.12 1.2374 B.22 C.12 1.2375 B.23 C.121.2376 B.24 C.12 1.2377 B.25 C.12 1.2378 B.26 C.12 1.2379 B.27 C.121.2380 B.28 C.12 1.2381 B.29 C.12 1.2382 B.30 C.12 1.2383 B.31 C.121.2384 B.32 C.12 1.2385 B.33 C.12 1.2386 B.34 C.12 1.2387 B.35 C.121.2388 B.36 C.12 1.2389 B.37 C.12 1.2390 B.38 C.12 1.2391 B.39 C.121.2392 B.40 C.12 1.2393 B.41 C.12 1.2394 B.42 C.12 1.2395 B.43 C.121.2396 B.44 C.12 1.2397 B.45 C.12 1.2398 B.46 C.12 1.2399 B.47 C.121.2400 B.48 C.12 1.2401 B.49 C.12 1.2402 B.50 C.12 1.2403 B.51 C.121.2404 B.52 C.12 1.2405 B.53 C.12 1.2406 B.54 C.12 1.2407 B.55 C.121.2408 B.56 C.12 1.2409 B.57 C.12 1.2410 B.58. C.12 1.2411 B.59 C.121.2412 B.60 C.12 1.2413 B.61 C.12 1.2414 B.62 C.12 1.2415 B.63 C.121.2416 B.64 C.12 1.2417 B.65 C.12 1.2418 B.66 C.12 1.2419 B.67 C.121.2420 B.68 C.12 1.2421 B.69 C.12 1.2422 B.70 C.12 1.2423 B.71 C.121.2424 B.72 C.12 1.2425 B.73 C.12 1.2426 B.74 C.12 1.2427 B.75 C.121.2428 B.76 C.12 1.2429 B.77 C.12 1.2430 B.78 C.12 1.2431 B.79 C.121.2432 B.80 C.12 1.2433 B.81 C.12 1.2434 B.82 C.12 1.2435 B.83 C.121.2436 B.84 C.12 1.2437 B.85 C.12 1.2438 B.86 C.12 1.2439 B.87 C.121.2440 B.88 C.12 1.2441 B.89 C.12 1.2442 B.90 C.12 1.2443 B.91 C.121.2444 B.92 C.12 1.2445 B.93 C.12 1.2446 B.94 C.12 1.2447 B.95 C.121.2448 B.96 C.12 1.2449 B.97 C.12 1.2450 B.98 C.12 1.2451 B.99 C.121.2452 B.100 C.12 1.2453 B.101 C.12 1.2454 B.102 C.12 1.2455 B.103 C.121.2456 B.104 C.12 1.2457 B.105 C.12 1.2458 B.106 C.12 1.2459 B.107 C.121.2460 B.108 C.12 1.2461 B.109 C.12 1.2462 B.110 C.12 1.2463 B.111 C.121.2464 B.112 C.12 1.2465 B.113 C.12 1.2466 B.114 C.12 1.2467 B.115 C.121.2468 B.116 C.12 1.2469 B.117 C.12 1.2470 B.118 C.12 1.2471 B.119 C.121.2472 B.120 C.12 1.2473 B.121 C.12 1.2474 B.122 C.12 1.2475 B.123 C.121.2476 B.124 C.12 1.2477 B.125 C.12 1.2478 B.126 C.12 1.2479 B.127 C.121.2480 B.128 C.12 1.2481 B.129 C.12 1.2482 B.130 C.12 1.2483 B.131 C.121.2484 B.132 C.12 1.2485 B.133 C.12 1.2486 B.134 C.12 1.2487 B.135 C.121.2488 B.136 C.12 1.2489 B.137 C.12 1.2490 B.138 C.12 1.2491 B.139 C.121.2492 B.140 C.12 1.2493 B.141 C.12 1.2494 B.142 C.12 1.2495 B.143 C.121.2496 B.144 C.12 1.2497 B.145 C.12 1.2498 B.146 C.12 1.2499 B.147 C.121.2500 B.148 C.12 1.2501 B.149 C.12 1.2502 B.150 C.12 1.2503 B.151 C.121.2504 B.152 C.12 1.2505 B.153 C.12 1.2506 B.154 C.12 1.2507 B.155 C.121.2508 B.156 C.12 1.2509 B.157 C.12 1.2510 B.158 C.12 1.2511 B.159 C.121.2512 B.160 C.12 1.2513 B.161 C.12 1.2514 B.162 C.12 1.2515 B.163 C.121.2516 B.164 C.12 1.2517 B.165 C.12 1.2518 B.166 C.12 1.2519 B.167 C.121.2520 B.168 C.12 1.2521 B.169 C.12 1.2522 B.170 C.12 1.2523 B.171 C.121.2524 B.172 C.12 1.2525 B.173 C.12 1.2526 B.174 C.12 1.2527 B.175 C.121.2528 B.176 C.12 1.2529 B.177 C.12 1.2530 B.178 C.12 1.2531 B.179 C.121.2532 B.180 C.12 1.2533 B.181 C.12 1.2534 B.182 C.12 1.2535 B.183 C.121.2536 B.184 C.12 1.2537 B.185 C.12 1.2538 B.186 C.12 1.2539 B.187 C.121.2540 B.188 C.12 1.2541 B.189 C.12 1.2542 B.190 C.12 1.2543 B.191 C.121.2544 B.192 C.12 1.2545 B.193 C.12 1.2546 B.194 C.12 1.2547 B.195 C.121.2548 B.196 C.12 1.2549 B.1 C.13 1.2550 B.2 C.13 1.2551 B.3 C.13 1.2552B.4 C.13 1.2553 B.5 C.13 1.2554 B.6 C.13 1.2555 B.7 C.13 1.2556 B.8 C.131.2557 B.9 C.13 1.2558 B.10 C.13 1.2559 B.11 C.13 1.2560 B.12 C.131.2561 B.13 C.13 1.2562 B.14 C.13 1.2563 B.15 C.13 1.2564 B.16 C.131.2565 B.17 C.13 1.2566 B.18 C.13 1.2567 B.19 C.13 1.2568 B.20 C.131.2569 B.21 C.13 1.2570 B.22 C.13 1.2571 B.23 C.13 1.2572 B.24 C.131.2573 B.25 C.13 1.2574 B.26 C.13 1.2575 B.27 C.13 1.2576 B.28 C.131.2577 B.29 C.13 1.2578 B.30 C.13 1.2579 B.31 C.13 1.2580 B.32 C.131.2581 B.33 C.13 1.2582 B.34 C.13 1.2583 B.35 C.13 1.2584 B.36 C.131.2585 B.37 C.13 1.2586 B.38 C.13 1.2587 B.39 C.13 1.2588 B.40 C.131.2589 B.41 C.13 1.2590 B.42 C.13 1.2591 B.43 C.13 1.2592 B.44 C.131.2593 B.45 C.13 1.2594 B.46 C.13 1.2595 B.47 C.13 1.2596 B.48 C.131.2597 B.49 C.13 1.2598 B.50 C.13 1.2599 B.51 C.13 1.2600 B.52 C.131.2601 B.53 C.13 1.2602 B.54 C.13 1.2603 B.55 C.13 1.2604 B.56 C.131.2605 B.57 C.13 1.2606 B.58. C.13 1.2607 B.59 C.13 1.2608 B.60 C.131.2609 B.61 C.13 1.2610 B.62 C.13 1.2611 B.63 C.13 1.2612 B.64 C.131.2613 B.65 C.13 1.2614 B.66 C.13 1.2615 B.67 C.13 1.2616 B.68 C.131.2617 B.69 C.13 1.2618 B.70 C.13 1.2619 B.71 C.13 1.2620 B.72 C.131.2621 B.73 C.13 1.2622 B.74 C.13 1.2623 B.75 C.13 1.2624 B.76 C.131.2625 B.77 C.13 1.2626 B.78 C.13 1.2627 B.79 C.13 1.2628 B.80 C.131.2629 B.81 C.13 1.2630 B.82 C.13 1.2631 B.83 C.13 1.2632 B.84 C.131.2633 B.85 C.13 1.2634 B.86 C.13 1.2635 B.87 C.13 1.2636 B.88 C.131.2637 B.89 C.13 1.2638 B.90 C.13 1.2639 B.91 C.13 1.2640 B.92 C.131.2641 B.93 C.13 1.2642 B.94 C.13 1.2643 B.95 C.13 1.2644 B.96 C.131.2645 B.97 C.13 1.2646 B.98 C.13 1.2647 B.99 C.13 1.2648 B.100 C.131.2649 B.101 C.13 1.2650 B.102 C.13 1.2651 B.103 C.13 1.2652 B.104 C.131.2653 B.105 C.13 1.2654 B.106 C.13 1.2655 B.107 C.13 1.2656 B.108 C.131.2657 B.109 C.13 1.2658 B.110 C.13 1.2659 B.111 C.13 1.2660 B.112 C.131.2661 B.113 C.13 1.2662 B.114 C.13 1.2663 B.115 C.13 1.2664 B.116 C.131.2665 B.117 C.13 1.2666 B.118 C.13 1.2667 B.119 C.13 1.2668 B.120 C.131.2669 B.121 C.13 1.2670 B.122 C.13 1.2671 B.123 C.13 1.2672 B.124 C.131.2673 B.125 C.13 1.2674 B.126 C.13 1.2675 B.127 C.13 1.2676 B.128 C.131.2677 B.129 C.13 1.2678 B.130 C.13 1.2679 B.131 C.13 1.2680 B.132 C.131.2681 B.133 C.13 1.2682 B.134 C.13 1.2683 B.135 C.13 1.2684 B.136 C.131.2685 B.137 C.13 1.2686 B.138 C.13 1.2687 B.139 C.13 1.2688 B.140 C.131.2689 B.141 C.13 1.2690 B.142 C.13 1.2691 B.143 C.13 1.2692 B.144 C.131.2693 B.145 C.13 1.2694 B.146 C.13 1.2695 B.147 C.13 1.2696 B.148 C.131.2697 B.149 C.13 1.2698 B.150 C.13 1.2699 B.151 C.13 1.2700 B.152 C.131.2701 B.153 C.13 1.2702 B.154 C.13 1.2703 B.155 C.13 1.2704 B.156 C.131.2705 B.157 C.13 1.2706 B.158 C.13 1.2707 B.159 C.13 1.2708 B.160 C.131.2709 B.161 C.13 1.2710 B.162 C.13 1.2711 B.163 C.13 1.2712 B.164 C.131.2713 B.165 C.13 1.2714 B.166 C.13 1.2715 B.167 C.13 1.2716 B.168 C.131.2717 B.169 C.13 1.2718 B.170 C.13 1.2719 B.171 C.13 1.2720 B.172 C.131.2721 B.173 C.13 1.2722 B.174 C.13 1.2723 B.175 C.13 1.2724 B.176 C.131.2725 B.177 C.13 1.2726 B.178 C.13 1.2727 B.179 C.13 1.2728 B.180 C.131.2729 B.181 C.13 1.2730 B.182 C.13 1.2731 B.183 C.13 1.2732 B.184 C.131.2733 B.185 C.13 1.2734 B.186 C.13 1.2735 B.187 C.13 1.2736 B.188 C.131.2737 B.189 C.13 1.2738 B.190 C.13 1.2739 B.191 C.13 1.2740 B.192 C.131.2741 B.193 C.13 1.2742 B.194 C.13 1.2743 B.195 C.13 1.2744 B.196 C.131.2745 B.1 C.14 1.2746 B.2 C.14 1.2747 B.3 C.14 1.2748 B.4 C.14 1.2749B.5 C.14 1.2750 B.6 C.14 1.2751 B.7 C.14 1.2752 B.8 C.14 1.2753 B.9 C.141.2754 B.10 C.14 1.2755 B.11 C.14 1.2756 B.12 C.14 1.2757 B.13 C.141.2758 B.14 C.14 1.2759 B.15 C.14 1.2760 B.16 C.14 1.2761 B.17 C.141.2762 B.18 C.14 1.2763 B.19 C.14 1.2764 B.20 C.14 1.2765 B.21 C.141.2766 B.22 C.14 1.2767 B.23 C.14 1.2768 B.24 C.14 1.2769 B.25 C.141.2770 B.26 C.14 1.2771 B.27 C.14 1.2772 B.28 C.14 1.2773 B.29 C.141.2774 B.30 C.14 1.2775 B.31 C.14 1.2776 B.32 C.14 1.2777 B.33 C.141.2778 B.34 C.14 1.2779 B.35 C.14 1.2780 B.36 C.14 1.2781 B.37 C.141.2782 B.38 C.14 1.2783 B.39 C.14 1.2784 B.40 C.14 1.2785 B.41 C.141.2786 B.42 C.14 1.2787 B.43 C.14 1.2788 B.44 C.14 1.2789 B.45 C.141.2790 B.46 C.14 1.2791 B.47 C.14 1.2792 B.48 C.14 1.2793 B.49 C.141.2794 B.50 C.14 1.2795 B.51 C.14 1.2796 B.52 C.14 1.2797 B.53 C.141.2798 B.54 C.14 1.2799 B.55 C.14 1.2800 B.56 C.14 1.2801 B.57 C.141.2802 B.58. C.14 1.2803 B.59 C.14 1.2804 B.60 C.14 1.2805 B.61 C.141.2806 B.62 C.14 1.2807 B.63 C.14 1.2808 B.64 C.14 1.2809 B.65 C.141.2810 B.66 C.14 1.2811 B.67 C.14 1.2812 B.68 C.14 1.2813 B.69 C.141.2814 B.70 C.14 1.2815 B.71 C.14 1.2816 B.72 C.14 1.2817 B.73 C.141.2818 B.74 C.14 1.2819 B.75 C.14 1.2820 B.76 C.14 1.2821 B.77 C.141.2822 B.78 C.14 1.2823 B.79 C.14 1.2824 B.80 C.14 1.2825 B.81 C.141.2826 B.82 C.14 1.2827 B.83 C.14 1.2828 B.84 C.14 1.2829 B.85 C.141.2830 B.86 C.14 1.2831 B.87 C.14 1.2832 B.88 C.14 1.2833 B.89 C.141.2834 B.90 C.14 1.2835 B.91 C.14 1.2836 B.92 C.14 1.2837 B.93 C.141.2838 B.94 C.14 1.2839 B.95 C.14 1.2840 B.96 C.14 1.2841 B.97 C.141.2842 B.98 C.14 1.2843 B.99 C.14 1.2844 B.100 C.14 1.2845 B.101 C.141.2846 B.102 C.14 1.2847 B.103 C.14 1.2848 B.104 C.14 1.2849 B.105 C.141.2850 B.106 C.14 1.2851 B.107 C.14 1.2852 B.108 C.14 1.2853 B.109 C.141.2854 B.110 C.14 1.2855 B.111 C.14 1.2856 B.112 C.14 1.2857 B.113 C.141.2858 B.114 C.14 1.2859 B.115 C.14 1.2860 B.116 C.14 1.2861 B.117 C.141.2862 B.118 C.14 1.2863 B.119 C.14 1.2864 B.120 C.14 1.2865 B.121 C.141.2866 B.122 C.14 1.2867 B.123 C.14 1.2868 B.124 C.14 1.2869 B.125 C.141.2870 B.126 C.14 1.2871 B.127 C.14 1.2872 B.128 C.14 1.2873 B.129 C.141.2874 B.130 C.14 1.2875 B.131 C.14 1.2876 B.132 C.14 1.2877 B.133 C.141.2878 B.134 C.14 1.2879 B.135 C.14 1.2880 B.136 C.14 1.2881 B.137 C.141.2882 B.138 C.14 1.2883 B.139 C.14 1.2884 B.140 C.14 1.2885 B.141 C.141.2886 B.142 C.14 1.2887 B.143 C.14 1.2888 B.144 C.14 1.2889 B.145 C.141.2890 B.146 C.14 1.2891 B.147 C.14 1.2892 B.148 C.14 1.2893 B.149 C.141.2894 B.150 C.14 1.2895 B.151 C.14 1.2896 B.152 C.14 1.2897 B.153 C.141.2898 B.154 C.14 1.2899 B.155 C.14 1.2900 B.156 C.14 1.2901 B.157 C.141.2902 B.158 C.14 1.2903 B.159 C.14 1.2904 B.160 C.14 1.2905 B.161 C.141.2906 B.162 C.14 1.2907 B.163 C.14 1.2908 B.164 C.14 1.2909 B.165 C.141.2910 B.166 C.14 1.2911 B.167 C.14 1.2912 B.168 C.14 1.2913 B.169 C.141.2914 B.170 C.14 1.2915 B.171 C.14 1.2916 B.172 C.14 1.2917 B.173 C.141.2918 B.174 C.14 1.2919 B.175 C.14 1.2920 B.176 C.14 1.2921 B.177 C.141.2922 B.178 C.14 1.2923 B.179 C.14 1.2924 B.180 C.14 1.2925 B.181 C.141.2926 B.182 C.14 1.2927 B.183 C.14 1.2928 B.184 C.14 1.2929 B.185 C.141.2930 B.186 C.14 1.2931 B.187 C.14 1.2932 B.188 C.14 1.2933 B.189 C.141.2934 B.190 C.14 1.2935 B.191 C.14 1.2936 B.192 C.14 1.2937 B.193 C.141.2938 B.194 C.14 1.2939 B.195 C.14 1.2940 B.196 C.14 1.2941 B.1 C.151.2942 B.2 C.15 1.2943 B.3 C.15 1.2944 B.4 C.15 1.2945 B.5 C.15 1.2946B.6 C.15 1.2947 B.7 C.15 1.2948 B.8 C.15 1.2949 B.9 C.15 1.2950 B.10C.15 1.2951 B.11 C.15 1.2952 B.12 C.15 1.2953 B.13 C.15 1.2954 B.14 C.151.2955 B.15 C.15 1.2956 B.16 C.15 1.2957 B.17 C.15 1.2958 B.18 C.151.2959 B.19 C.15 1.2960 B.20 C.15 1.2961 B.21 C.15 1.2962 B.22 C.151.2963 B.23 C.15 1.2964 B.24 C.15 1.2965 B.25 C.15 1.2966 B.26 C.151.2967 B.27 C.15 1.2968 B.28 C.15 1.2969 B.29 C.15 1.2970 B.30 C.151.2971 B.31 C.15 1.2972 B.32 C.15 1.2973 B.33 C.15 1.2974 B.34 C.151.2975 B.35 C.15 1.2976 B.36 C.15 1.2977 B.37 C.15 1.2978 B.38 C.151.2979 B.39 C.15 1.2980 B.40 C.15 1.2981 B.41 C.15 1.2982 B.42 C.151.2983 B.43 C.15 1.2984 B.44 C.15 1.2985 B.45 C.15 1.2986 B.46 C.151.2987 B.47 C.15 1.2988 B.48 C.15 1.2989 B.49 C.15 1.2990 B.50 C.151.2991 B.51 C.15 1.2992 B.52 C.15 1.2993 B.53 C.15 1.2994 B.54 C.151.2995 B.55 C.15 1.2996 B.56 C.15 1.2997 B.57 C.15 1.2998 B.58. C.151.2999 B.59 C.15 1.3000 B.60 C.15 1.3001 B.61 C.15 1.3002 B.62 C.151.3003 B.63 C.15 1.3004 B.64 C.15 1.3005 B.65 C.15 1.3006 B.66 C.151.3007 B.67 C.15 1.3008 B.68 C.15 1.3009 B.69 C.15 1.3010 B.70 C.151.3011 B.71 C.15 1.3012 B.72 C.15 1.3013 B.73 C.15 1.3014 B.74 C.151.3015 B.75 C.15 1.3016 B.76 C.15 1.3017 B.77 C.15 1.3018 B.78 C.151.3019 B.79 C.15 1.3020 B.80 C.15 1.3021 B.81 C.15 1.3022 B.82 C.151.3023 B.83 C.15 1.3024 B.84 C.15 1.3025 B.85 C.15 1.3026 B.86 C.151.3027 B.87 C.15 1.3028 B.88 C.15 1.3029 B.89 C.15 1.3030 B.90 C.151.3031 B.91 C.15 1.3032 B.92 C.15 1.3033 B.93 C.15 1.3034 B.94 C.151.3035 B.95 C.15 1.3036 B.96 C.15 1.3037 B.97 C.15 1.3038 B.98 C.151.3039 B.99 C.15 1.3040 B.100 C.15 1.3041 B.101 C.15 1.3042 B.102 C.151.3043 B.103 C.15 1.3044 B.104 C.15 1.3045 B.105 C.15 1.3046 B.106 C.151.3047 B.107 C.15 1.3048 B.108 C.15 1.3049 B.109 C.15 1.3050 B.110 C.151.3051 B.111 C.15 1.3052 B.112 C.15 1.3053 B.113 C.15 1.3054 B.114 C.151.3055 B.115 C.15 1.3056 B.116 C.15 1.3057 B.117 C.15 1.3058 B.118 C.151.3059 B.119 C.15 1.3060 B.120 C.15 1.3061 B.121 C.15 1.3062 B.122 C.151.3063 B.123 C.15 1.3064 B.124 C.15 1.3065 B.125 C.15 1.3066 B.126 C.151.3067 B.127 C.15 1.3068 B.128 C.15 1.3069 B.129 C.15 1.3070 B.130 C.151.3071 B.131 C.15 1.3072 B.132 C.15 1.3073 B.133 C.15 1.3074 B.134 C.151.3075 B.135 C.15 1.3076 B.136 C.15 1.3077 B.137 C.15 1.3078 B.138 C.151.3079 B.139 C.15 1.3080 B.140 C.15 1.3081 B.141 C.15 1.3082 B.142 C.151.3083 B.143 C.15 1.3084 B.144 C.15 1.3085 B.145 C.15 1.3086 B.146 C.151.3087 B.147 C.15 1.3088 B.148 C.15 1.3089 B.149 C.15 1.3090 B.150 C.151.3091 B.151 C.15 1.3092 B.152 C.15 1.3093 B.153 C.15 1.3094 B.154 C.151.3095 B.155 C.15 1.3096 B.156 C.15 1.3097 B.157 C.15 1.3098 B.158 C.151.3099 B.159 C.15 1.3100 B.160 C.15 1.3101 B.161 C.15 1.3102 B.162 C.151.3103 B.163 C.15 1.3104 B.164 C.15 1.3105 B.165 C.15 1.3106 B.166 C.151.3107 B.167 C.15 1.3108 B.168 C.15 1.3109 B.169 C.15 1.3110 B.170 C.151.3111 B.171 C.15 1.3112 B.172 C.15 1.3113 B.173 C.15 1.3114 B.174 C.151.3115 B.175 C.15 1.3116 B.176 C.15 1.3117 B.177 C.15 1.3118 B.178 C.151.3119 B.179 C.15 1.3120 B.180 C.15 1.3121 B.181 C.15 1.3122 B.182 C.151.3123 B.183 C.15 1.3124 B.184 C.15 1.3125 B.185 C.15 1.3126 B.186 C.151.3127 B.187 C.15 1.3128 B.188 C.15 1.3129 B.189 C.15 1.3130 B.190 C.151.3131 B.191 C.15 1.3132 B.192 C.15 1.3133 B.193 C.15 1.3134 B.194 C.151.3135 B.195 C.15 1.3136 B.196 C.15 1.3137 B.1 C.16 1.3138 B.2 C.161.3139 B.3 C.16 1.3140 B.4 C.16 1.3141 B.5 C.16 1.3142 B.6 C.16 1.3143B.7 C.16 1.3144 B.8 C.16 1.3145 B.9 C.16 1.3146 B.10 C.16 1.3147 B.11C.16 1.3148 B.12 C.16 1.3149 B.13 C.16 1.3150 B.14 C.16 1.3151 B.15 C.161.3152 B.16 C.16 1.3153 B.17 C.16 1.3154 B.18 C.16 1.3155 B.19 C.161.3156 B.20 C.16 1.3157 B.21 C.16 1.3158 B.22 C.16 1.3159 B.23 C.161.3160 B.24 C.16 1.3161 B.25 C.16 1.3162 B.26 C.16 1.3163 B.27 C.161.3164 B.28 C.16 1.3165 B.29 C.16 1.3166 B.30 C.16 1.3167 B.31 C.161.3168 B.32 C.16 1.3169 B.33 C.16 1.3170 B.34 C.16 1.3171 B.35 C.161.3172 B.36 C.16 1.3173 B.37 C.16 1.3174 B.38 C.16 1.3175 B.39 C.161.3176 B.40 C.16 1.3177 B.41 C.16 1.3178 B.42 C.16 1.3179 B.43 C.161.3180 B.44 C.16 1.3181 B.45 C.16 1.3182 B.46 C.16 1.3183 B.47 C.161.3184 B.48 C.16 1.3185 B.49 C.16 1.3186 B.50 C.16 1.3187 B.51 C.161.3188 B.52 C.16 1.3189 B.53 C.16 1.3190 B.54 C.16 1.3191 B.55 C.161.3192 B.56 C.16 1.3193 B.57 C.16 1.3194 B.58. C.16 1.3195 B.59 C.161.3196 B.60 C.16 1.3197 B.61 C.16 1.3198 B.62 C.16 1.3199 B.63 C.161.3200 B.64 C.16 1.3201 B.65 C.16 1.3202 B.66 C.16 1.3203 B.67 C.161.3204 B.68 C.16 1.3205 B.69 C.16 1.3206 B.70 C.16 1.3207 B.71 C.161.3208 B.72 C.16 1.3209 B.73 C.16 1.3210 B.74 C.16 1.3211 B.75 C.161.3212 B.76 C.16 1.3213 B.77 C.16 1.3214 B.78 C.16 1.3215 B.79 C.161.3216 B.80 C.16 1.3217 B.81 C.16 1.3218 B.82 C.16 1.3219 B.83 C.161.3220 B.84 C.16 1.3221 B.85 C.16 1.3222 B.86 C.16 1.3223 B.87 C.161.3224 B.88 C.16 1.3225 B.89 C.16 1.3226 B.90 C.16 1.3227 B.91 C.161.3228 B.92 C.16 1.3229 B.93 C.16 1.3230 B.94 C.16 1.3231 B.95 C.161.3232 B.96 C.16 1.3233 B.97 C.16 1.3234 B.98 C.16 1.3235 B.99 C.161.3236 B.100 C.16 1.3237 B.101 C.16 1.3238 B.102 C.16 1.3239 B.103 C.161.3240 B.104 C.16 1.3241 B.105 C.16 1.3242 B.106 C.16 1.3243 B.107 C.161.3244 B.108 C.16 1.3245 B.109 C.16 1.3246 B.110 C.16 1.3247 B.111 C.161.3248 B.112 C.16 1.3249 B.113 C.16 1.3250 B.114 C.16 1.3251 B.115 C.161.3252 B.116 C.16 1.3253 B.117 C.16 1.3254 B.118 C.16 1.3255 B.119 C.161.3256 B.120 C.16 1.3257 B.121 C.16 1.3258 B.122 C.16 1.3259 B.123 C.161.3260 B.124 C.16 1.3261 B.125 C.16 1.3262 B.126 C.16 1.3263 B.127 C.161.3264 B.128 C.16 1.3265 B.129 C.16 1.3266 B.130 C.16 1.3267 B.131 C.161.3268 B.132 C.16 1.3269 B.133 C.16 1.3270 B.134 C.16 1.3271 B.135 C.161.3272 B.136 C.16 1.3273 B.137 C.16 1.3274 B.138 C.16 1.3275 B.139 C.161.3276 B.140 C.16 1.3277 B.141 C.16 1.3278 B.142 C.16 1.3279 B.143 C.161.3280 B.144 C.16 1.3281 B.145 C.16 1.3282 B.146 C.16 1.3283 B.147 C.161.3284 B.148 C.16 1.3285 B.149 C.16 1.3286 B.150 C.16 1.3287 B.151 C.161.3288 B.152 C.16 1.3289 B.153 C.16 1.3290 B.154 C.16 1.3291 B.155 C.161.3292 B.156 C.16 1.3293 B.157 C.16 1.3294 B.158 C.16 1.3295 B.159 C.161.3296 B.160 C.16 1.3297 B.161 C.16 1.3298 B.162 C.16 1.3299 B.163 C.161.3300 B.164 C.16 1.3301 B.165 C.16 1.3302 B.166 C.16 1.3303 B.167 C.161.3304 B.168 C.16 1.3305 B.169 C.16 1.3306 B.170 C.16 1.3307 B.171 C.161.3308 B.172 C.16 1.3309 B.173 C.16 1.3310 B.174 C.16 1.3311 B.175 C.161.3312 B.176 C.16 1.3313 B.177 C.16 1.3314 B.178 C.16 1.3315 B.179 C.161.3316 B.180 C.16 1.3317 B.181 C.16 1.3318 B.182 C.16 1.3319 B.183 C.161.3320 B.184 C.16 1.3321 B.185 C.16 1.3322 B.186 C.16 1.3323 B.187 C.161.3324 B.188 C.16 1.3325 B.189 C.16 1.3326 B.190 C.16 1.3327 B.191 C.161.3328 B.192 C.16 1.3329 B.193 C.16 1.3330 B.194 C.16 1.3331 B.195 C.161.3332 B.196 C.16 1.3333 B.1 C.17 1.3334 B.2 C.17 1.3335 B.3 C.17 1.3336B.4 C.17 1.3337 B.5 C.17 1.3338 B.6 C.17 1.3339 B.7 C.17 1.3340 B.8 C.171.3341 B.9 C.17 1.3342 B.10 C.17 1.3343 B.11 C.17 1.3344 B.12 C.171.3345 B.13 C.17 1.3346 B.14 C.17 1.3347 B.15 C.17 1.3348 B.16 C.171.3349 B.17 C.17 1.3350 B.18 C.17 1.3351 B.19 C.17 1.3352 B.20 C.171.3353 B.21 C.17 1.3354 B.22 C.17 1.3355 B.23 C.17 1.3356 B.24 C.171.3357 B.25 C.17 1.3358 B.26 C.17 1.3359 B.27 C.17 1.3360 B.28 C.171.3361 B.29 C.17 1.3362 B.30 C.17 1.3363 B.31 C.17 1.3364 B.32 C.171.3365 B.33 C.17 1.3366 B.34 C.17 1.3367 B.35 C.17 1.3368 B.36 C.171.3369 B.37 C.17 1.3370 B.38 C.17 1.3371 B.39 C.17 1.3372 B.40 C.171.3373 B.41 C.17 1.3374 B.42 C.17 1.3375 B.43 C.17 1.3376 B.44 C.171.3377 B.45 C.17 1.3378 B.46 C.17 1.3379 B.47 C.17 1.3380 B.48 C.171.3381 B.49 C.17 1.3382 B.50 C.17 1.3383 B.51 C.17 1.3384 B.52 C.171.3385 B.53 C.17 1.3386 B.54 C.17 1.3387 B.55 C.17 1.3388 B.56 C.171.3389 B.57 C.17 1.3390 B.58. C.17 1.3391 B.59 C.17 1.3392 B.60 C.171.3393 B.61 C.17 1.3394 B.62 C.17 1.3395 B.63 C.17 1.3396 B.64 C.171.3397 B.65 C.17 1.3398 B.66 C.17 1.3399 B.67 C.17 1.3400 B.68 C.171.3401 B.69 C.17 1.3402 B.70 C.17 1.3403 B.71 C.17 1.3404 B.72 C.171.3405 B.73 C.17 1.3406 B.74 C.17 1.3407 B.75 C.17 1.3408 B.76 C.171.3409 B.77 C.17 1.3410 B.78 C.17 1.3411 B.79 C.17 1.3412 B.80 C.171.3413 B.81 C.17 1.3414 B.82 C.17 1.3415 B.83 C.17 1.3416 B.84 C.171.3417 B.85 C.17 1.3418 B.86 C.17 1.3419 B.87 C.17 1.3420 B.88 C.171.3421 B.89 C.17 1.3422 B.90 C.17 1.3423 B.91 C.17 1.3424 B.92 C.171.3425 B.93 C.17 1.3426 B.94 C.17 1.3427 B.95 C.17 1.3428 B.96 C.171.3429 B.97 C.17 1.3430 B.98 C.17 1.3431 B.99 C.17 1.3432 B.100 C.171.3433 B.101 C.17 1.3434 B.102 C.17 1.3435 B.103 C.17 1.3436 B.104 C.171.3437 B.105 C.17 1.3438 B.106 C.17 1.3439 B.107 C.17 1.3440 B.108 C.171.3441 B.109 C.17 1.3442 B.110 C.17 1.3443 B.111 C.17 1.3444 B.112 C.171.3445 B.113 C.17 1.3446 B.114 C.17 1.3447 B.115 C.17 1.3448 B.116 C.171.3449 B.117 C.17 1.3450 B.118 C.17 1.3451 B.119 C.17 1.3452 B.120 C.171.3453 B.121 C.17 1.3454 B.122 C.17 1.3455 B.123 C.17 1.3456 B.124 C.171.3457 B.125 C.17 1.3458 B.126 C.17 1.3459 B.127 C.17 1.3460 B.128 C.171.3461 B.129 C.17 1.3462 B.130 C.17 1.3463 B.131 C.17 1.3464 B.132 C.171.3465 B.133 C.17 1.3466 B.134 C.17 1.3467 B.135 C.17 1.3468 B.136 C.171.3469 B.137 C.17 1.3470 B.138 C.17 1.3471 B.139 C.17 1.3472 B.140 C.171.3473 B.141 C.17 1.3474 B.142 C.17 1.3475 B.143 C.17 1.3476 B.144 C.171.3477 B.145 C.17 1.3478 B.146 C.17 1.3479 B.147 C.17 1.3480 B.148 C.171.3481 B.149 C.17 1.3482 B.150 C.17 1.3483 B.151 C.17 1.3484 B.152 C.171.3485 B.153 C.17 1.3486 B.154 C.17 1.3487 B.155 C.17 1.3488 B.156 C.171.3489 B.157 C.17 1.3490 B.158 C.17 1.3491 B.159 C.17 1.3492 B.160 C.171.3493 B.161 C.17 1.3494 B.162 C.17 1.3495 B.163 C.17 1.3496 B.164 C.171.3497 B.165 C.17 1.3498 B.166 C.17 1.3499 B.167 C.17 1.3500 B.168 C.171.3501 B.169 C.17 1.3502 B.170 C.17 1.3503 B.171 C.17 1.3504 B.172 C.171.3505 B.173 C.17 1.3506 B.174 C.17 1.3507 B.175 C.17 1.3508 B.176 C.171.3509 B.177 C.17 1.3510 B.178 C.17 1.3511 B.179 C.17 1.3512 B.180 C.171.3513 B.181 C.17 1.3514 B.182 C.17 1.3515 B.183 C.17 1.3516 B.184 C.171.3517 B.185 C.17 1.3518 B.186 C.17 1.3519 B.187 C.17 1.3520 B.188 C.171.3521 B.189 C.17 1.3522 B.190 C.17 1.3523 B.191 C.17 1.3524 B.192 C.171.3525 B.193 C.17 1.3526 B.194 C.17 1.3527 B.195 C.17 1.3528 B.196 C.171.3529 — C.1 1.3530 — C.2 1.3531 — C.3 1.3532 — C.4 1.3533 — C.5 1.3534— C.6 1.3535 — C.7 1.3536 — C.8 1.3537 — C.9 1.3538 — C.10 1.3539 — C.111.3540 — C.12 1.3541 — C.13 1.3542 — C.14 1.3543 — C.15 1.3544 — C.161.3545 — C.17

The specific number for each single composition is deductible asfollows: Composition 1.200 for example comprises compounds of formula(I) cyhalofop-butyl (B.4) and benoxacor (C.1).

Composition 2.200 for example comprises the compounds of formula (I)(see the definition for compositions 2.1 to 2.3545 below),cyhalofop-butyl (B.4) and benoxacor (C.1).

Composition 7.200 for example comprises compounds of formula (I)imazapyr (B.35), cyhalofop-butyl (B.4) and benoxacor (C.1.

Also especially preferred are compositions 2.1. to 2.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theycomprise as the active compound A the compounds of formula (Ia).

Also especially preferred are compositions 3.1. to 3.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.2 clodinafop-propargyl as further herbicide B.

Also especially preferred are compositions 4.1. to 4.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.8 pinoxaden as further herbicide B.

Also especially preferred are compositions 5.1. to 5.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.30 imazamox as further herbicide B.

Also especially preferred are compositions 6.1. to 6.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.32 imazapic as further herbicide B.

Also especially preferred are compositions 7.1. to 7.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.35 imazapyr as further herbicide B.

Also especially preferred are compositions 8.1. to 8.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.38 imazaquin as further herbicide B.

Also especially preferred are compositions 9.1. to 9.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.40 imazethapyr as further herbicide B.

Also especially preferred are compositions 10.1. to 10.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.51 nicosulfuron as further herbicide B.

Also especially preferred are compositions 11.1. to 11.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.55 pyribenzoxim as further herbicide B.

Also especially preferred are compositions 12.1. to 12.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.56 pyriftalid as further herbicide B.

Also especially preferred are compositions 13.1. to 13.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.64 tritosulfuron as further herbicide B.

Also especially preferred are compositions 14.1. to 14.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.66 ametryne as further herbicide B.

Also especially preferred are compositions 15.1. to 15.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.67 atrazine as further herbicide B.

Also especially preferred are compositions 16.1. to 16.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.68 bentazon as further herbicide B.

Also especially preferred are compositions 17.1. to 17.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.69 bromoxynil as further herbicide B.

Also especially preferred are compositions 18.1. to 18.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.73 diuron as further herbicide B.

Also especially preferred are compositions 19.1. to 19.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.76 isoproturon as further herbicide B.

Also especially preferred are compositions 20.1. to 20.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.81 simazin as further herbicide B.

Also especially preferred are compositions 21.1. to 21.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.82 terbuthylazin as further herbicide B.

Also especially preferred are compositions 22.1. to 22.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.85 acifluorfen as further herbicide B.

Also especially preferred are compositions 23.1. to 23.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.88 flumioxazin as further herbicide B.

Also especially preferred are compositions 24.1. to 24.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.89 fomesafen as further herbicide B.

Also especially preferred are compositions 25.1. to 25.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.94 saflufenacil as further herbicide B.

Also especially preferred are compositions 26.1. to 26.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.95 sulfentrazone as further herbicide B.

Also especially preferred are compositions 27.1. to 27.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.98 benzbicyclone as further herbicide B.

Also especially preferred are compositions 28.1. to 28.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.100 clomazone as further herbicide B.

Also especially preferred are compositions 29.1. to 29.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.103 isoxaflutole as further herbicide B.

Also especially preferred are compositions 30.1. to 30.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.103 isoxaflutole and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 31.1. to 31.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.103 isoxaflutole and B.76 isoproturon as furtherherbicides B.

Also especially preferred are compositions 32.1. to 32.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.103 isoxaflutole and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 33.1. to 33.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.104 mesotrione as further herbicide B.

Also especially preferred are compositions 34.1. to 34.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.104 mesotrione and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 35.1. to 35.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.104 mesotrione and B.76 isoproturon as furtherherbicides B.

Also especially preferred are compositions 36.1. to 36.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.104 mesotrione and B.82 terbutylazin as furtherherbicides B.

Also especially preferred are compositions 37.1. to 37.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.106 picolinafen as further herbicide B.

Also especially preferred are compositions 38.1. to 38.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.107 sulcotrione as further herbicide B.

Also especially preferred are compositions 39.1. to 39.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B. 107 sulcotrione and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 40.1. to 40.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B. 107 sulcotrione and B.76 isoproturon as furtherherbicides B.

Also especially preferred are compositions 41.1. to 41.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B. 107 sulcotrione and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 42.1. to 42.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.109 tembotrione as further herbicide B.

Also especially preferred are compositions 43.1. to 43.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.111 topramezone as further herbicide B.

Also especially preferred are compositions 44.1. to 44.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.111 topramezone and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 45.1. to 45.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.111 topramezone and B.76 isoproturon as furtherherbicides B.

Also especially preferred are compositions 46.1. to 46.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.111 topramezone and B.82 terbutylazin as furtherherbicides B.

Also especially preferred are compositions 47.1. to 47.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.116 glyphosate as further herbicide B.

Also especially preferred are compositions 48.1. to 48.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.116 glyphosate and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 49.1. to 49.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.116 glyphosate and B.94 saflufenacil as furtherherbicides B.

Also especially preferred are compositions 50.1. to 50.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.116 glyphosate and B.103 isoxaflutole as furtherherbicides B.

Also especially preferred are compositions 51.1. to 51.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.116 glyphosate and B.128 acetochlor as furtherherbicides B.

Also especially preferred are compositions 52.1. to 52.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.116 glyphosate and B.104 mesotrione as furtherherbicides B.

Also especially preferred are compositions 53.1. to 53.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.116 glyphosate and B.107 sulcotrione as furtherherbicides B.

Also especially preferred are compositions 54.1. to 54.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.116 glyphosate and B.111 topramezone as furtherherbicides B.

Also especially preferred are compositions 55.1. to 55.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.122 glufosinate as further herbicide B.

Also especially preferred are compositions 56.1. to 56.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.126 pendimethalin as further herbicide B.

Also especially preferred are compositions 57.1. to 57.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.128 acetochlor as further herbicide B.

Also especially preferred are compositions 58.1. to 58.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.131 dimethenamid-P as further herbicide B.

Also especially preferred are compositions 59.1. to 59.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.132 fentrazamide as further herbicide B.

Also especially preferred are compositions 60.1. to 60.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.133 flufenacet as further herbicide B.

Also especially preferred are compositions 61.1. to 61.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.135 metazachlor as further herbicide B.

Also especially preferred are compositions 62.1. to 62.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.137 S-metolachlor as further herbicide B.

Also especially preferred are compositions 63.1. to 63.3545 which differfrom the corresponding compositions 11.1 to 1.3545 only in that theyadditionally comprise B.138 pretilachlor as further herbicide B.

Also especially preferred are compositions 64.1. to 64.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.140 indaziflam as further herbicide B.

Also especially preferred are compositions 65.1. to 65.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.145 2,4-D as further herbicide B.

Also especially preferred are compositions 66.1. to 66.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.153 clopyralid as further herbicide B.

Also especially preferred are compositions 67.1. to 67.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.156 dicamba as further herbicide B.

Also especially preferred are compositions 68.1. to 68.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.171 MCPA as further herbicide B.

Also especially preferred are compositions 69.1. to 69.3545 which differfrom the corresponding compositions 1.1 to 1.3545 only in that theyadditionally comprise B.174 quinclorac as further herbicide B.

The invention also relates to agrochemical compositions comprising anauxiliary and at least one diaminotriazine compound of formula (I) or acomposition according to the invention.

An agrochemical diaminotriazine compound of formula (I) or a compositioncomprises a pesticidally effective amount of at least one compositionaccording to the invention. The term “effective amount” denotes anamount of the active ingredients, which is sufficient for controllingunwanted plants, especially for controlling unwanted plants incultivated plants and which does not result in a substantial damage tothe treated plants. Such an amount can vary in a broad range and isdependent on various factors, such as the plants to be controlled, thetreated cultivated plant or material, the climatic conditions and thespecific composition according to the invention used.

The diamonotriazine compounds of formula (I) (compounds A) andoptionally B and/or C, their N-oxides, salts or derivatives can beconverted into customary types of agrochemical compositions, e.g.solutions, emulsions, suspensions, dusts, powders, pastes, granules,pressings, capsules, and mixtures thereof. Examples for agrochemicalcomposition types are suspensions (e.g. SC, OD, FS), emulsifiableconcentrates (e.g. EC), emulsions (e.g. EW, EO, ES, ME), capsules (e.g.CS, ZC), pastes, pastilles, wettable powders or dusts (e.g. WP, SP, WS,DP, DS), pressings (e.g. BR, TB, DT), granules (e.g. WG, SG, GR, FG, GG,MG), insecticidal articles (e.g. LN), as well as gel formulations forthe treatment of plant propagation materials such as seeds (e.g. GF).These and further agrochemical compositions types are defined in the“Catalogue of pesticide formulation types and international codingsystem”, Technical Monograph No. 2, 6^(th) Ed. May 2008, CropLifeInternational.

The agrochemical compositions are prepared in a known manner, such asdescribed by Mollet and Grubemann, Formulation technology, Wiley VCH,Weinheim, 2001; or Knowles, New developments in crop protection productformulation, Agrow Reports DS243, T&F Informa, London, 2005.

Suitable auxiliaries are solvents, liquid carriers, solid carriers orfillers, surfactants, dispersants, emulsifiers, wetters, adjuvants,solubilizers, penetration enhancers, protective colloids, adhesionagents, thickeners, humectants, repellents, attractants, feedingstimulants, compatibilizers, bactericides, anti-freezing agents,anti-foaming agents, colorants, tackifiers and binders.

Suitable solvents and liquid carriers are water and organic solvents,such as mineral oil fractions of medium to high boiling point, e.g.kerosene, diesel oil; oils of vegetable or animal origin; aliphatic,cyclic and aromatic hydrocarbons, e.g. toluene, paraffin,tetrahydronaphthalene, alkylated naphthalenes; alcohols, e.g. ethanol,propanol, butanol, benzylalcohol, cyclohexanol; glycols; DMSO; ketones,e.g. cyclohexanone; esters, e.g. lactates, carbonates, fatty acidesters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides,e.g. N-methylpyrrolidone, fatty acid dimethylamides; and mixturesthereof.

Suitable solid carriers or fillers are mineral earths, e.g. silicates,silica gels, talc, kaolins, limestone, lime, chalk, clays, dolomite,diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate,magnesium oxide; polysaccharides, e.g. cellulose, starch; fertilizers,e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas;products of vegetable origin, e.g. cereal meal, tree bark meal, woodmeal, nutshell meal, and mixtures thereof.

Suitable surfactants are surface-active compounds, such as anionic,cationic, nonionic and amphoteric surfactants, block polymers,polyelectrolytes, and mixtures thereof. Such surfactants can be used asemulsifier, dispersant, solubilizer, wetter, penetration enhancer,protective colloid, or adjuvant. Examples of surfactants are listed inMcCutcheon's, Vol. 1: Emulsifiers & Detergents, McCutcheon'sDirectories, Glen Rock, USA, 2008 (International Ed. or North AmericanEd.).

Suitable anionic surfactants are alkali, alkaline earth or ammoniumsalts of sulfonates, sulfates, phosphates, carboxylates, and mixturesthereof. Examples of sulfonates are alkylarylsulfonates,diphenylsulfonates, alpha-olefin sulfonates, lignine sulfonates,sulfonates of fatty acids and oils, sulfonates of ethoxylatedalkylphenols, sulfonates of alkoxylated arylphenols, sulfonates ofcondensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes,sulfonates of naphthalenes and alkyl-naphthalenes, sulfosuccinates orsulfosuccinamates. Examples of sulfates are sulfates of fatty acids andoils, of ethoxylated alkylphenols, of alcohols, of ethoxylated alcohols,or of fatty acid esters. Examples of phosphates are phosphate esters.Examples of carboxylates are alkyl carboxylates, and carboxylatedalcohol or alkylphenol ethoxylates.

Suitable nonionic surfactants are alkoxylates, N-substituted fatty acidamides, amine oxides, esters, sugar-based surfactants, polymericsurfactants, and mixtures thereof. Examples of alkoxylates are compoundssuch as alcohols, alkylphenols, amines, amides, arylphenols, fatty acidsor fatty acid esters which have been alkoxylated with 1 to 50equivalents. Ethylene oxide and/or propylene oxide may be employed forthe alkoxylation, preferably ethylene oxide. Examples of N-substitutedfatty acid amides are fatty acid glucamides or fatty acid alkanolamides.Examples of esters are fatty acid esters, glycerol esters ormonoglycerides. Examples of sugar-based surfactants are sorbitans,ethoxylated sorbitans, sucrose and glucose esters oralkylpolyglucosides. Examples of polymeric surfactants are home- orcopolymers of vinylpyrrolidone, vinylalcohols, or vinylacetate.

Suitable cationic surfactants are quaternary surfactants, for examplequaternary ammonium compounds with one or two hydrophobic groups, orsalts of long-chain primary amines. Suitable amphoteric surfactants arealkylbetains and imidazolines. Suitable block polymers are blockpolymers of the A-B or A-B-A type comprising blocks of polyethyleneoxide and polypropylene oxide, or of the A-B—C type comprising alkanol,polyethylene oxide and polypropylene oxide. Suitable polyelectrolytesare polyacids or polybases. Examples of polyacids are alkali salts ofpolyacrylic acid or polyacid comb polymers. Examples of polybases arepolyvinylamines or polyethyleneamines.

Suitable adjuvants are compounds, which have a neglectable or even nopesticidal activity themselves, and which improve the biologicalperformance of the compound I on the target. Examples are surfactants,mineral or vegetable oils, and other auxiliaries. Further examples arelisted by Knowles, Adjuvants and additives, Agrow Reports DS256, T&FInforma UK, 2006, chapter 5.

Suitable thickeners are polysaccharides (e.g. xanthan gum,carboxymethylcellulose), inorganic clays (organically modified orunmodified), polycarboxylates, and silicates.

Suitable bactericides are bronopol and isothiazolinone derivatives suchas alkylisothiazolinones and benzisothiazolinones.

Suitable anti-freezing agents are ethylene glycol, propylene glycol,urea and glycerin.

Suitable anti-foaming agents are silicones, long chain alcohols, andsalts of fatty acids.

Suitable colorants (e.g. in red, blue, or green) are pigments of lowwater solubility and water-soluble dyes. Examples are inorganiccolorants (e.g. iron oxide, titan oxide, iron hexacyanoferrate) andorganic colorants (e.g. alizarin-, azo- and phthalocyanine colorants).

Suitable tackifiers or binders are polyvinylpyrrolidons,polyvinylacetates, polyvinyl alcohols, polyacrylates, biological orsynthetic waxes, and cellulose ethers.

Examples for agrochemical composition types and their preparation are:

i) Water-Soluble Concentrates (SL, LS)

10-60 wt % of a compound of formula (I) or compostion according to theinvention and 5-15 wt % wetting agent (e.g. alcohol alkoxylates) aredissolved in water and/or in a water-soluble solvent (e.g. alcohols) ad100 wt %. The active substance dissolves upon dilution with water.

ii) Dispersible Concentrates (DC)

5-25 wt % of a diamonitriazine compound of formula (I) or compositionaccording to the invention and 1-10 wt % dispersant (e. g.polyvinylpyrrolidone) are dissolved in organic solvent (e.g.cyclohexanone) ad 100 wt %. Dilution with water gives a dispersion.

iii) Emulsifiable Concentrates (EC)

15-70 wt % of a diamonitriazine compound of formula (I) or compositionaccording to the invention and 5-10 wt % emulsifiers (e.g. calciumdodecylbenzenesulfonate and castor oil ethoxylate) are dissolved inwater-insoluble organic solvent (e.g. aromatic hydrocarbon) ad 100 wt %.Dilution with water gives an emulsion.

iv) Emulsions (EW, EO, ES)

5-40 wt % of a diamonitriazine compound of formula (I) or compositionaccording to the invention and 1-10 wt % emulsifiers (e.g. calciumdodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in20-40 wt % water-insoluble organic solvent (e.g. aromatic hydrocarbon).This mixture is introduced into water ad 100 wt % by means of anemulsifying machine and made into a homogeneous emulsion. Dilution withwater gives an emulsion.

v) Suspensions (SC, OD, FS)

In an agitated ball mill, 20-60 wt % of a diamonitriazine compound offormula (I) or composition according to the invention are comminutedwith addition of 2-10 wt % dispersants and wetting agents (e.g. sodiumlignosulfonate and alcohol ethoxylate), 0.1-2 wt % thickener (e.g.xanthan gum) and water ad 100 wt % to give a fine active substancesuspension. Dilution with water gives a stable suspension of the activesubstance. For FS type composition up to 40 wt % binder (e.g.polyvinylalcohol) is added.

vi) Water-Dispersible Granules and Water-Soluble Granules (WG, SG)

50-80 wt % of a diamonitriazine compound of formula (I) or compositionaccording to the invention are ground finely with addition ofdispersants and wetting agents (e.g. sodium lignosulfonate and alcoholethoxylate) ad 100 wt % and prepared as water-dispersible orwater-soluble granules by means of technical appliances (e. g.extrusion, spray tower, fluidized bed). Dilution with water gives astable dispersion or solution of the active substance.

vii) Water-Dispersible Powders and Water-Soluble Powders (WP, SP, WS)

50-80 wt % of a compound of formula (I) or composition according to theinvention are ground in a rotor-stator mill with addition of 1-5 wt %dispersants (e.g. sodium lignosulfonate), 1-3 wt % wetting agents (e.g.alcohol ethoxylate) and solid carrier (e.g. silica gel) ad 100 wt %.Dilution with water gives a stable dispersion or solution of the activesubstance.

viii) Gel (GW, GF)

In an agitated ball mill, 5-25 wt % of a diamonitriazine compound offormula (I) or a composition according to the invention are comminutedwith addition of 3-10 wt % dispersants (e.g. sodium lignosulfonate), 1-5wt % thickener (e.g. carboxymethylcellulose) and water ad 100 wt % togive a fine suspension of the active substance. Dilution with watergives a stable suspension of the active substance.

iv) Microemulsion (ME)

5-20 wt % of a diamonitriazine compound of formula (I) or a compositionaccording to the invention are added to 5-30 wt % organic solvent blend(e.g. fatty acid dimethylamide and cyclohexanone), 10-25 wt % surfactantblend (e.g. alcohol ethoxylate and arylphenol ethoxylate), and water ad100%. This mixture is stirred for 1 h to produce spontaneously athermodynamically stable microemulsion.

iv) Microcapsules (CS)

An oil phase comprising 5-50 wt % of a diamonitriazine compound offormula (I) or a composition according to the invention, 0-40 wt % waterinsoluble organic solvent (e.g. aromatic hydrocarbon), 2-15 wt % acrylicmonomers (e.g. methylmethacrylate, methacrylic acid and a di- ortriacrylate) are dispersed into an aqueous solution of a protectivecolloid (e.g. polyvinyl alcohol). Radical polymerization initiated by aradical initiator results in the formation of poly(meth)acrylatemicrocapsules. Alternatively, an oil phase comprising 5-50 wt % of adiamonitriazine compound of formula (I) according to the invention, 0-40wt % water insoluble organic solvent (e.g. aromatic hydrocarbon), and anisocyanate monomer (e.g. diphenylmethene-4,4′-diisocyanate) aredispersed into an aqueous solution of a protective colloid (e.g.polyvinyl alcohol). The addition of a polyamine (e.g.hexamethylenediamine) results in the formation of polyureamicrocapsules. The monomers amount to 1-10 wt %. The wt % relate to thetotal CS composition.

ix) Dustable Powders (DP, DS)

1-10 wt % of a diamonitriazine compound of formula (I) or a compositionaccording to the invention are ground finely and mixed intimately withsolid carrier (e.g. finely divided kaolin) ad 100 wt %.

x) Granules (GR, FG)

0.5-30 wt % of a diamonitriazine compound of formula (I) or acomposition according to the invention is ground finely and associatedwith solid carrier (e.g. silicate) ad 100 wt %. Granulation is achievedby extrusion, spray-drying or the fluidized bed.

xi) Ultra-Low Volume Liquids (UL)

1-50 wt % of a diamonitriazine compound of formula (I) or a compositionaccording to the invention are dissolved in organic solvent (e.g.aromatic hydrocarbon) ad 100 wt %.

The agrochemical compositions types i) to xi) may optionally comprisefurther auxiliaries, such as 0.1-1 wt % bactericides, 5-15 wt %anti-freezing agents, 0.1-1 wt % anti-foaming agents, and 0.1-1 wt %colorants.

The agrochemical compositions generally comprise between 0.01 and 95%,preferably between 0.1 and 90%, and in particular between 0.5 and 75%,by weight of active substance. The active substances are employed in apurity of from 90% to 100%, preferably from 95% to 100% (according toNMR spectrum).

Solutions for seed treatment (LS), suspoemulsions (SE), flowableconcentrates (FS), powders for dry treatment (DS), water-dispersiblepowders for slurry treatment (WS), water-soluble powders (SS), emulsions(ES), emulsifiable concentrates (EC) and gels (GF) are usually employedfor the purposes of treatment of plant propagation materials,particularly seeds. The compositions in question give, aftertwo-to-tenfold dilution, active substance concentrations of from 0.01 to60% by weight, preferably from 0.1 to 40% by weight, in the ready-to-usepreparations. Application can be carried out before or during sowing.

Methods for applying diamonitriazine compounds of formula (I) andcompositions thereof, respectively, on to plant propagation material,especially seeds include dressing, coating, pelleting, dusting, soakingand in-furrow application methods of the propagation material.Preferably, compound I or the compositions thereof, respectively, areapplied on to the plant propagation material by a method such thatgermination is not induced, e. g. by seed dressing, pelleting, coatingand dusting.

Various types of oils, wetters, adjuvants, fertilizer, ormicronutrients, and further pesticides (e.g. herbicides, insecticides,fungicides, growth regulators, safeners) may be added to the activesubstances or the compositions comprising them as premix or, ifappropriate not until immediately prior to use (tank mix). These agentscan be admixed with the compositions according to the invention in aweight ratio of 1:100 to 100:1, preferably 1:10 to 10:1.

The user applies the agrochemical composition according to the inventionusually from a predosage device, a knapsack sprayer, a spray tank, aspray plane, or an irrigation system. Usually, the agrochemicalcomposition is made up with water, buffer, and/or further auxiliaries tothe desired application concentration and the ready-to-use spray liquoror the agrochemical composition according to the invention is thusobtained. Usually, 20 to 2000 liters, preferably 50 to 400 liters, ofthe ready-to-use spray liquor are applied per hectare of agriculturaluseful area.

According to one embodiment, either individual components of theagrochemical composition according to the invention or partiallypremixed components, e. g. agrochemical components comprising compoundsof formula (I) and/or active substances from the groups B and/or C maybe mixed by the user in a spray tank and further auxiliaries andadditives may be added, if appropriate.

In a further embodiment, individual components of the agrochemicalcomposition according to the invention such as parts of a kit or partsof a binary or ternary mixture may be mixed by the user himself in aspray tank and further auxiliaries may be added, if appropriate.

In a further embodiment, either individual components of theagrochemical composition according to the invention or partiallypremixed components, e. g. components comprising compounds of formula(I) and active substances from the groups B and/or C, can be appliedjointly (e.g. after tank mix) or consecutively.

Accordingly, a first embodiment of the invention relates to compositionsin the form of a agrochemical composition formulated as a 1-componentcomposition comprising the at least one active compound of formula (I)or the at least one active compound of formula (I) (active compound A)and at least one further active compound selected from the herbicides Band the safeners C and also a solid or liquid carrier and, ifappropriate, one or more surfactants.

Accordingly, a second embodiment of the invention relates tocompositions in the form of a agrochemical composition formulated as a2-component composition comprising a first formulation (component)comprising the at least one active compound A, which is a compound offormula (I), a solid or liquid carrier and, if appropriate, one or moresurfactants, and a second component comprising at least one furtheractive compound selected from the herbicides B and safeners C, a solidor liquid carrier and, if appropriate, one or more surfactants.

The active compound A, which is a compound of formula (I) and the atleast one further active compound B and/or C can be formulated andapplied jointly or separately, simultaneously or in succession, before,during or after the emergence of the plants. In case of separateapplication, the order of the application of the active compounds A, Band/or C is of minor importance. The only thing that is important isthat the at least one active compound A and the at least one furtheractive compound B and/or C are present simultaneously at the site ofaction, i.e. are at the same time in contact with or taken up by theplant to be controlled or to be safened.

The compounds of formula (I) or compositions according to the inventionare suitable as herbicides. They are suitable as such or as anappropriately formulated composition (agrochemical composition).

The compounds of formula (I) or compositions according to the inventioncontrol vegetation on non-crop areas very efficiently, especially athigh rates of application. They act against broad-leafed weeds and grassweeds in crops such as wheat, rice, corn, soybeans and cotton withoutcausing any significant damage to the crop plants. This effect is mainlyobserved at low rates of application.

The compounds of formula (I) or compositions according to the inventionare applied to the plants mainly by spraying the leaves. Here, theapplication can be carried out using, for example, water as carrier bycustomary spraying techniques using spray liquor amounts of from about100 to 1000 I/ha (for example from 300 to 400 I/ha). The herbicidalcompositions may also be applied by the low-volume or theultra-low-volume method, or in the form of microgranules.

Application of the compounds of formula (I) or herbicidal compositionsaccording to the present invention can be done before, during and/orafter, preferably during and/or after, the emergence of the undesirableplants.

The compounds of formula (I) or herbicidal compositions according to thepresent invention can be applied pre- or post-emergence or together withthe seed of a crop plant. It is also possible to apply the compounds andcompositions by applying seed, pretreated with a composition of theinvention, of a crop plant. If the active compounds A and B and, ifappropriate C, are less well tolerated by certain crop plants,application techniques may be used in which the herbicidal compositionsare sprayed, with the aid of the spraying equipment, in such a way thatas far as possible they do not come into contact with the leaves of thesensitive crop plants, while the active compounds reach the leaves ofundesirable plants growing underneath, or the bare soil surface(post-directed, lay-by).

In a further embodiment, the composition according to the invention canbe applied by treating seed. The treatment of seed comprises essentiallyall procedures familiar to the person skilled in the art (seed dressing,seed coating, seed dusting, seed soaking, seed film coating, seedmultilayer coating, seed encrusting, seed dripping and seed pelleting)based on the compounds of the formula (I) according to the invention orthe compositions prepared therefrom. Here, the herbicidal compositionscan be applied diluted or undiluted.

The term “seed” comprises seed of all types, such as, for example,corns, seeds, fruits, tubers, seedlings and similar forms. Here,preferably, the term seed describes corns and seeds. The seed used canbe seed of the useful plants mentioned above, but also the seed oftransgenic plants or plants obtained by customary breeding methods.

Moreover, it may be advantageous to apply the compounds of formula (I)or compositions of the present invention on their own or jointly incombination with other crop protection agents, for example with agentsfor controlling pests or phytopathogenic fungi or bacteria or withgroups of active compounds which regulate growth. Also of interest isthe miscibility with mineral salt solutions which are employed fortreating nutritional and trace element deficiencies. Non-phytotoxic oilsand oil concentrates can also be added.

When employed in plant protection, the amounts of active substancesapplied, i.e. A (compounds of formula (I)) and B and, if appropriate, Cwithout formulation auxiliaries, are, depending on the kind of effectdesired, from 0.001 to 2 kg per ha, preferably from 0.005 to 2 kg perha, more preferably from 0.05 to 0.9 kg per ha and in particular from0.1 to 0.75 kg per ha.

In another embodiment of the invention, the application rate of A(compounds of formula (I)) and B and, if appropriate, C, is from 0.001to 3 kg/ha, preferably from 0.005 to 2.5 kg/ha and in particular from0.01 to 2 kg/ha of active substance (a.s.).

In another preferred embodiment of the invention, the rates ofapplication of the compounds of formula (I) according to the presentinvention (total amount of compounds of formula (I)) are from 0.1 g/hato 3000 g/ha, preferably 10 g/ha to 1000 g/ha, depending on the controltarget, the season, the target plants and the growth stage.

In another preferred embodiment of the invention, the application ratesof the compounds of formula (I) are in the range from 0.1 g/ha to 5000g/ha and preferably in the range from 1 g/ha to 2500 g/ha or from 5 g/hato 2000 g/ha.

In another preferred embodiment of the invention, the application rateof the compounds of formula (I) is 0.1 to 1000 g/ha, preferablyl to 750g/ha, more preferably 5 to 500 g/ha.

The required application rates of herbicidal compounds B are generallyin the range of from 0.0005 kg/ha to 2.5 kg/ha and preferably in therange of from 0.005 kg/ha to 2 kg/ha or 0.01 kg/ha to 1.5 kg/h of a.s.

The required application rates of safeners C are generally in the rangeof from 0.0005 kg/ha to 2.5 kg/ha and preferably in the range of from0.005 kg/ha to 2 kg/ha or 0.01 kg/ha to 1.5 kg/h of a.s.

In treatment of plant propagation materials such as seeds, e. g. bydusting, coating or drenching seed, amounts of active substance of from0.1 to 1000 g, preferably from 1 to 1000 g, more preferably from 1 to100 g and most preferably from 5 to 100 g, per 100 kilogram of plantpropagation material (preferably seeds) are generally required.

In another embodiment of the invention, to treat the seed, the amountsof active substances applied, i.e. A and B and, if appropriate, C aregenerally employed in amounts of from 0.001 to 10 kg per 100 kg of seed.

When used in the protection of materials or stored products, the amountof active substance applied depends on the kind of application area andon the desired effect.

Amounts customarily applied in the protection of materials are 0.001 gto 2 kg, preferably 0.005 g to 1 kg, of active substance per cubic meterof treated material.

In the methods of the present invention it is immaterial whether theherbicide compound A of formula (I), and the further herbicide componentB and/or the herbicide safener compound C are formulated and appliedjointly or separately.

In the case of separate application it is of minor importance, in whichorder the application takes place. It is only necessary, that theherbicide compound A and the herbicide compound B and/or the herbicidesafener compound C are applied in a time frame that allows simultaneousaction of the active ingredients on the plants, preferably within atime-frame of at most 14 days, in particular at most 7 days.

Depending on the application method in question, the compositionsaccording to the invention can additionally be employed in a furthernumber of crop plants for eliminating undesirable plants. Examples ofsuitable crops are the following: Allium cepa, Ananas comosus, Arachishypogaea, Asparagus officinalis, Avena sativa, Beta vulgaris spec.altissima, Beta vulgaris spec. rapa, Brassica napus var. napus, Brassicanapus var. napobrassica, Brassica rapa var. silvestris, Brassicaoleracea, Brassica nigra, Camellia sinensis, Carthamus tinctorius, Caryaillinoinensis, Citrus limon, Citrus sinensis, Coffea arabica (Coffeacanephora, Coffea liberica), Cucumis sativus, Cynodon dactylon, Daucuscarota, Elaeis guineensis, Fragaria vesca, Glycine max, Gossypiumhirsutum, (Gossypium arboreum, Gossypium herbaceum, Gossypiumvitifolium), Helianthus annuus, Hevea brasiliensis, Hordeum vulgare,Humulus lupulus, Ipomoea batatas, Juglans regia, Lens culinaris, Linumusitatissimum, Lycopersicon lycopersicum, Malus spec., Manihotesculenta, Medicago sativa, Musa spec., Nicotiana tabacum (N.rustica),Olea europaea, Oryza sativa, Phaseolus lunatus, Phaseolus vulgaris,Picea abies, Pinus spec., Pistacia vera, Pisum sativum, Prunus avium,Prunus persica, Pyrus communis, Prunus armeniaca, Prunus cerasus, Prunusdulcis and prunus domestica, Ribes sylvestre, Ricinus communis,Saccharum officinarum, Secale cereale, Sinapis alba, Solanum tuberosum,Sorghum bicolor (s. vulgare), Theobroma cacao, Trifolium pratense,Triticum aestivum, Triticale, Triticum durum, Vicia faba, Vitisvinifera, Zea mays.

Preferred crops are Arachis hypogaea, Beta vulgaris spec. altissima,Brassica napus var. napus, Brassica oleracea, Citrus limon, Citrussinensis, Coffea arabica (Coffea canephora, Coffea liberica), Cynodondactylon, Glycine max, Gossypium hirsutum, (Gossypium arboreum,Gossypium herbaceum, Gossypium vitifolium), Helianthus annuus, Hordeumvulgare, Juglans regia, Lens culinaris, Linum usitatissimum,Lycopersicon lycopersicum, Malus spec., Medicago sativa, Nicotianatabacum (N.rustica), Olea europaea, Oryza sativa, Phaseolus lunatus,Phaseolus vulgaris, Pistacia vera, Pisum sativum, Prunus dulcis,Saccharum officinarum, Secale cereale, Solanum tuberosum, Sorghumbicolor (s. vulgare), Triticale, Triticum aestivum, Triticum durum,Vicia faba, Vitis vinifera and Zea mays

Especially preferred crops are crops of cereals, corn, soybeans, rice,oilseed rape, cotton, potatoes, peanuts or permanent crops.

The compositions according to the invention can also be used ingenetically modified plants. The term “genetically modified plants” isto be understood as plants whose genetic material has been modified bythe use of recombinant DNA techniques to include an inserted sequence ofDNA that is not native to that plant species' genome or to exhibit adeletion of DNA that was native to that species' genome, wherein themodification(s) cannot readily be obtained by cross breeding,mutagenesis or natural recombination alone. Often, a particulargenetically modified plant will be one that has obtained its geneticmodification(s) by inheritance through a natural breeding or propagationprocess from an ancestral plant whose genome was the one directlytreated by use of a recombinant DNA technique. Typically, one or moregenes have been integrated into the genetic material of a geneticallymodified plant in order to improve certain properties of the plant. Suchgenetic modifications also include but are not limited to targetedpost-translational modification of protein(s), oligo- or polypeptides.e.g., by inclusion therein of amino acid mutation(s) that permit,decrease, or promote glycosylation or polymer additions such asprenylation, acetylation farnesylation, or PEG moiety attachment.

Plants that have been modified by breeding, mutagenesis or geneticengineering, e.g. have been rendered tolerant to applications ofspecific classes of herbicides, such as auxinic herbicides such asdicamba or 2,4-D; bleacher herbicides such as 4-hydroxyphenylpyruvatedioxygenase (HPPD) inhibitors or phytoene desaturase (PDS) inhibitors;acetolactate synthase (ALS) inhibitors such as sulfonylureas orimidazolinones; enolpyruvyl shikimate 3-phosphate synthase (EPSP)inhibitors such as glyphosate; glutamine synthetase (GS) inhibitors suchas glufosinate; protoporphyrinogen-IX oxidase inhibitors; lipidbiosynthesis inhibitors such as acetylCoA carboxylase (ACCase)inhibitors; or oxynil (i. e. bromoxynil or ioxynil) herbicides as aresult of conventional methods of breeding or genetic engineering;furthermore, plants have been made resistant to multiple classes ofherbicides through multiple genetic modifications, such as resistance toboth glyphosate and glufosinate or to both glyphosate and a herbicidefrom another class such as ALS inhibitors, HPPD inhibitors, auxinicherbicides, or ACCase inhibitors. These herbicide resistancetechnologies are, for example, described in Pest Management Science 61,2005, 246; 61, 2005, 258; 61, 2005, 277; 61, 2005, 269; 61, 2005, 286;64, 2008, 326; 64, 2008, 332; Weed Science 57, 2009, 108; AustralianJournal of Agricultural Research 58, 2007, 708; Science 316, 2007, 1185;and references quoted therein. Several cultivated plants have beenrendered tolerant to herbicides by mutagenesis and conventional methodsof breeding, e. g., Clearfield® summer rape (Canola, BASF SE, Germany)being tolerant to imidazolinones, e. g., imazamox, or ExpressSun®sunflowers (DuPont, USA) being tolerant to sulfonyl ureas, e. g.,tribenuron. Genetic engineering methods have been used to rendercultivated plants such as soybean, cotton, corn, beets and rape,tolerant to herbicides such as glyphosate, imidazolinones andglufosinate, some of which are under development or commerciallyavailable under the brands or trade names RoundupReady® (glyphosatetolerant, Monsanto, USA), Cultivance® (imidazolinone tolerant, BASF SE,Germany) and LibertyLink® (glufosinate tolerant, Bayer CropScience,Germany).

Furthermore, plants are also covered that are by the use of recombinantDNA techniques capable to synthesize one or more insecticidal proteins,especially those known from the bacterial genus Bacillus, particularlyfrom Bacillus thuringiensis, such as delta-endotoxins, e. g., CryIA(b),CryIA(c), CryIF, CryIF(a2), CryIIA(b), CryIIIA, CryIIIB(b1) or Cry9c;vegetative insecticidal proteins (VIP), e. g., VIP1, VIP2, VIP3 orVIP3A; insecticidal proteins of bacteria colonizing nematodes, e. g.,Photorhabdus spp. or Xenorhabdus spp.; toxins produced by animals, suchas scorpion toxins, arachnid toxins, wasp toxins, or otherinsect-specific neurotoxins; toxins produced by fungi, such asStreptomycetes toxins, plant lectins, such as pea or barley lectins;agglutinins; proteinase inhibitors, such as trypsin inhibitors, serineprotease inhibitors, patatin, cystatin or papain inhibitors;ribosome-inactivating proteins (RIP), such as ricin, maize-RIP, abrin,luffin, saporin or bryodin; steroid metabolism enzymes, such as3-hydroxy-steroid oxidase, ecdysteroid-IDP-glycosyl-transferase,cholesterol oxidases, ecdysone inhibitors or HMG-CoA-reductase; ionchannel blockers, such as blockers of sodium or calcium channels;juvenile hormone esterase; diuretic hormone receptors (helicokininreceptors); stilbene synthase, bibenzyl synthase, chitinases orglucanases. In the context of the present invention these insecticidalproteins or toxins are to be understood expressly also as includingpre-toxins, hybrid proteins, truncated or otherwise modified proteins.Hybrid proteins are characterized by a new combination of proteindomains, (see, e. g., WO 02/015701). Further examples of such toxins orgenetically modified plants capable of synthesizing such toxins aredisclosed, e. g., in EP-A 374 753, WO 93/007278, WO 95/34656, EP-A 427529, EP-A 451 878, WO 03/18810 und WO 03/52073. The methods forproducing such genetically modified plants are generally known to theperson skilled in the art and are described, e. g., in the publicationsmentioned above. These insecticidal proteins contained in thegenetically modified plants impart to the plants producing theseproteins tolerance to harmful pests from all taxonomic groups ofarthropods, especially to beetles (Coleoptera), two-winged insects(Diptera), and moths (Lepidoptera) and to nematodes (Nematoda).Genetically modified plants capable to synthesize one or moreinsecticidal proteins are, e. g., described in the publicationsmentioned above, and some of which are commercially available such asYieldGard® (corn cultivars producing the CryIAb toxin), YieldGard® Plus(corn cultivars producing CryIAb and Cry3Bb1 toxins), Starlink® (corncultivars producing the Cry9c toxin), Herculex® RW (corn cultivarsproducing Cry34Ab1, Cry35Ab1 and the enzymePhosphinothricin-N-Acetyltransferase [PAT]); NuCOTN® 33B (cottoncultivars producing the CryIAc toxin), Bollgard® I (cotton cultivarsproducing the CryIAc toxin), Bollgard® II (cotton cultivars producingCryIAc and Cry2Ab2 toxins); VIPCOT® (cotton cultivars producing aVIP-toxin); NewLeaf® (potato cultivars producing the Cry3A toxin);Bt-Xtra®, NatureGard®, KnockOut®, BiteGard®, Protecta®, Btl 1 (e. g.,Agrisure® CB) and Bt176 from Syngenta Seeds SAS, France, (corn cultivarsproducing the CryIAb toxin and PAT enzyme), MIR604 from Syngenta SeedsSAS, France (corn cultivars producing a modified version of the Cry3Atoxin, c.f. WO 03/018810), MON 863 from Monsanto Europe S.A., Belgium(corn cultivars producing the Cry3Bb1 toxin), IPC 531 from MonsantoEurope S.A., Belgium (cotton cultivars producing a modified version ofthe CryIAc toxin) and 1507 from Pioneer Overseas Corporation, Belgium(corn cultivars producing the Cry1F toxin and PAT enzyme).

Furthermore, plants are also covered that are by the use of recombinantDNA techniques capable to synthesize one or more proteins to increasethe resistance or tolerance of those plants to bacterial, viral orfungal pathogens. Examples of such proteins are the so-called“pathogenesis-related proteins” (PR proteins, see, e.g., EP-A 392 225),plant disease resistance genes (e. g., potato cultivars, which expressresistance genes acting against Phytophthora infestans derived from theMexican wild potato, Solanum bulbocastanum) or T4-lysozym (e.g., potatocultivars capable of synthesizing these proteins with increasedresistance against bacteria such as Erwinia amylovora). The methods forproducing such genetically modified plants are generally known to theperson skilled in the art and are described, e.g., in the publicationsmentioned above.

Furthermore, plants are also covered that are by the use of recombinantDNA techniques capable to synthesize one or more proteins to increasethe productivity (e.g., bio-mass production, grain yield, starchcontent, oil content or protein content), tolerance to drought, salinityor other growth-limiting environmental factors or tolerance to pests andfungal, bacterial or viral pathogens of those plants.

Furthermore, plants are also covered that contain by the use ofrecombinant DNA techniques a modified amount of ingredients or newingredients, specifically to improve human or animal nutrition, e. g.,oil crops that produce health-promoting long-chain omega-3 fatty acidsor unsaturated omega-9 fatty acids (e. g., Nexera® rape, DowAgroSciences, Canada).

Furthermore, plants are also covered that contain by the use ofrecombinant DNA techniques a modified amount of ingredients or newingredients, specifically to improve raw material production, e.g.,potatoes that produce increased amounts of amylopectin (e.g. Amflora®potato, BASF SE, Germany).

Furthermore, it has been found that the the compositions according tothe invention are also suitable for the defoliation and/or desiccationof plant parts, for which crop plants such as cotton, potato, oilseedrape, sunflower, soybean or field beans, in particular cotton, aresuitable. In this regard compositions have been found for thedesiccation and/or defoliation of plants, processes for preparing thesecompositions, and methods for desiccating and/or defoliating plantsusing the compositions according to the invention.

As desiccants, the compositions according to the invention are suitablein particular for desiccating the above-ground parts of crop plants suchas potato, oilseed rape, sunflower and soybean, but also cereals. Thismakes possible the fully mechanical harvesting of these important cropplants.

Also of economic interest is the facilitation of harvesting, which ismade possible by concentrating within a certain period of time thedehiscence, or reduction of adhesion to the tree, in citrus fruit,olives and other species and varieties of pomaceous fruit, stone fruitand nuts. The same mechanism, i.e. the promotion of the development ofabscission tissue between fruit part or leaf part and shoot part of theplants is also essential for the controlled defoliation of usefulplants, in particular cotton.

Moreover, a shortening of the time interval in which the individualcotton plants mature leads to an increased fiber quality afterharvesting.

-   -   Another aspect of the invention is an agrochemical composition        comprising a herbicidal active amount of at least one compound        of formula (I) as defined above and at least one inert liquid        and/or solid carrier and, if appropriate, at least one        surface-active substances.    -   A further aspect of the invention is a method of controlling        undesired vegetation, which comprises allowing a herbicidally        active amount of at least one compound of formula (I) as as        defined above to act on plants, their environment or on seed.    -   A further aspect of the invention in is the use of a compound of        formula (I) as defined aboven as a herbicide or for the        desiccation/defoliation of plants.

The preparation of the diaminotriazine compounds of formula (I) isillustrated by examples; however, the subject matter of the presentinvention is not limited to the examples given.

The products shown below were characterized by the mass ([m/z]) orretention time (RT; [min.]) determined by HPLC-MS spectrometry or by¹H-NMR.

HPLC-MS=high performance liquid chromatography-coupled massspectrometry; HPLC column:

RP-18 column (Chromolith Speed ROD from Merck KgaA, Germany), 50*4.6 mm;mobile phase: acetonitrile+0.1% trifluoroacetic acid (TFA)/water+0.1%TFA using a gradient from 5:95 to 100:0 over 5 minutes at 40° C., flowrate 1.8 ml/min. MS: quadrupole electrospray ionization, 80 V (positivemode)

The following abbreviations are used:

TFA: Trifluoroacetic acid

CH: Cyclohexane

EtOAc: Ethyl acetate

THF: Tetrahydrofurane DMF: N,N-Dimethylformamide MeOH: Methanol

HPLC: High pressure chromatographyLC: Liquid chromatographyMS: Mass spectrometryaq.: aqueousPd/C: Palladium on charcoals singlets_(br) broad singletd dublettt triplettq quartettm multiplettdt doublet of triplett

A PREPARATION EXAMPLES Example 1N2-[2-(cyclopentoxy)-6-fluoro-phenyl]-6-(1-fluoro-1-methyl-ethyl)-1,3,5-triazine-2,4-diamine

Step 1:1-(cyclopentoxy)-3-fluoro-2-nitro-benzene

A suspension of cyclopentanol (1.62 g, 18.8 mmol),1,3-difluoro-2-nitro-benzene (1.5 g, 9.42 mmol) and Cs₂CO₃ (6.14 g, 18.8mmol) in DMF (30 mL) was heated at 100° C. over night. The resultingmixture was diluted with water and EtOAc and afterwards the phases wereseparated. The water phase was further extracted with EtOAc (2×) and theorganic phases were combined, dried over anhydrous Na₂SO₄ and thesolvent was removed. Purification by column chromatography (gradient:100% CH to 4:1 CH: EtOAc) afforded the desired compound (900 mg, 4 mmol,42%).

¹H NMR (CDCl₃, 400 MHz): δ=7.32 (m, 1H), 6.79 (d, 1H, J=8.7 Hz), 6.74(dt, 1H, J=8.7, 0.9 Hz), 4.85 (q, 1H, J=4.0 Hz), 1.85 (m, 4H), 1.75 (m,2H), 1.59 (m, 2H).

Step 2: 2-(cyclopentoxy)-6-fluoro-aniline

Powdered Pd/C (10%, 300 mg) was added to a solution of1-(cyclopentoxy)-3-fluoro-2-nitro-benzene (900 mg, 4 mmol) in methanol(100 mL) and the resulting mixture was stirred under H₂ pressure for 2 hat ambient temperature. The mixture was filtered through Celite® whilebeing rinsed with methanol. The combined solutions were evaporated togive the crude title coumpound (730 mg, 3.74 mmol, 94%), which was usedin the next step without further purification.

¹H NMR (CDCl₃, 400 MHz): δ=6.61 (m, 3H), 4.78 (m, 1H), 3.69 (brs, 2H,NH₂), 1.89 (m, 4H), 1.80 (m, 2H), 1.63 (m, 2H).

Step 3:1-carbamimidoyl-3-[2-(cyclopentoxy)-6-fluoro-phenyl]guanidine

Aq. HCl (38% w/w, 1 mL) was added, with stirring, to a solution of2-(cyclopentoxy)-6-fluoro-aniline (0.73 g, 3.74 mmol) and2-cyanoguanidine (0.38 g, 4.5 mmol) in acetonitrile (50 mL). The mixturewas heated under microwave radiation (140° C., 15 bar) for 45 min. Aftercooling to ambient temperature aq. NaOH (2 mol/L) was added until a pHof 12 was reached. Ethyl acetate was added to the mixture and the phaseswere separated. The organic phase was dried over anhydrous Na₂SO₄ andconcentrated under reduced pressure. The resulting crude product (0.88g, 3.16 mol, 84%) was used without further purification in the nextstep.

MS (ESI) m/z=279.4 [M+H⁺].

Step 4:N2-[2-(cyclopentoxy)-6-fluoro-phenyl]-6-(1-fluoro-1-methyl-ethyl)-1,3,5-triazine-2,4-diamine

2-Fluoro-2-methyl-propanoyl chloride (0.39 g, 3.13 mmol) was slowlyadded, with stirring, to a solution of1-carbamimidoyl-3-[2-(cyclopentoxy)-6-fluoro-phenyl]guanidine (0.88 g,3.15 mmol) and triethylamine (1.3 mL, 9.45 mmol) in THF (30 mL). Theresulting mixture was heated at 60° C. for 6 hours. The reaction mixturewas cooled to ambient temperature, diluted with water and ethyl acetate,and the phases were separated. After washing the aqueous phase withEtOAc the combined organic phases were washed with brine, dried overanhydreous Na₂SO₄, filtered and concentrated under reduced pressure.Column chromatography of the resulting crude product (gradient: 100% CHto 1:1 CH: EtOAc) afforded the desired product (120 mg, 0.34 mmol, 11%).

¹H NMR (CDCl₃, 400 MHz): δ=7.13 (m, 1H), 6.72 (m, 2H), 6.60 (brs, 1H,NH), 5.42 (brs, 2H, NH₂), 4.76 (sept, 1H, J=3.0 Hz), 1.84 (m, 4H), 1.69(m, 2H), 1.67 (s, 3H), 1.62 (s, 3H), 1.58 (m, 2H).

The HPLC-MS data for the compound prepared according to Example 1 aregiven in the following table C. Also included in table C are the datafor compounds of Examples 2 and 3 which have been prepared by analogy tothe procedures described above for Example 1 and are depicted as formula(I′) below.

TABLE C RT MS ¹⁾ No. R^(a) R³ R⁴ R⁵ [min] [m/z] 1 cyclopentyloxy F CH₃CH₃ 0.980 349.9 2 (cyclopropyl)methyloxy F CH₃ CH₃ 0.927 335.8 3cyclohexyloxy F CH₃ CH₃ 1.032 363.8 ¹⁾ Mass Spectrum M⁺ or [M + H]⁺[m/z]

B USE EXAMPLES

The herbicidal activity of the azines of formula (I) was demonstrated bythe following greenhouse experiments:

The culture containers used were plastic flowerpots containing loamysand with approximately 3.0% of humus as the substrate. The seeds of thetest plants were sown separately for each species.

For the pre-emergence treatment, the active ingredients, which had beensuspended or emulsified in water, were applied directly after sowing bymeans of finely distributing nozzles. The containers were irrigatedgently to promote germination and growth and subsequently covered withtransparent plastic hoods until the plants had rooted. This cover causeduniform germination of the test plants, unless this had been impaired bythe active ingredients.

For the post-emergence treatment, the test plants were first grown to aheight of 3 to 15 cm, depending on the plant habit, and only thentreated with the active ingredients which had been suspended oremulsified in water. For this purpose, the test plants were either sowndirectly and grown in the same containers, or they were first grownseparately as seedlings and transplanted into the test containers a fewdays prior to treatment.

Depending on the species, the plants were kept at 10-25° C. or 20-35°C., respectively.

The test period extended over 2 to 4 weeks. During this time, the plantswere tended, and their response to the individual treatments wasevaluated.

Evaluation was carried out using a scale from 0 to 100. 100 means noemergence of the plants, or complete destruction of at least the aerialmoieties, and 0 means no damage, or normal course of growth. A moderateherbicidal activity is given at values of at least 60, a good herbicidalactivity is given at values of at least 70, and a very good herbicidalactivity is given at values of at least 85.

The plants used in the greenhouse experiments were of the followingspecies:

Bayer code Scientific name ABUTH Abutilon theophrasti AMARE Amaranthusretroflexus APESV Apera spica-venti

Example 1 applied by pre-emergence method at an application rate of0.250 kg/ha, showed very good herbicidal activity against AMARE and goodherbicidal activity against APESV.

Example 2 applied by pre-emergence method at an application rate of0.250 kg/ha, showed very good herbicidal activity against ABUTH, AMAREand APESV.

1-17. (canceled)
 18. A diaminotriazine compound of formula (I)

wherein q is 0, 1, 2 or 3 R^(a) is selected from the group consisting ofC₁-C₆-haloalkoxy, C₁-C₆-haloalkylthio, (C₁-C₆-haloalkyl)sulfinyl,(C₁-C₆-haloalkyl)-carbonyl, (C₁-C₆-haloalkyl)sulfonyl, C₂-C₆-alkenyloxy,C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy, C₂-C₆-haloalkynyloxy,(C₁-C₆-haloalkoxy)-C₁-C₆-alkoxy, (C₁-C₆-alkyl)-carbonyloxy,(C₁-C₆-haloalkyl)-carbonyloxy, C₃-C₆-cycloalkoxy, C₃-C₆-halocycloalkoxy,(C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy, (C₃-C₆-halocycloalkyl)-C₁-C₄-alkoxy,(C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, (C₃-C₆-halocycloalkyl)-C₁-C₄-alkyl,(C₃-C₆-cycloalkoxy)-C₁-C₄-alkyl, (C₃-C₆-halocycloalkoxy)-C₁-C₄-alkyl,(C₃-C₆-cycloalkyl)-carbonyloxy, (C₁-C₆-alkoxy)-C₁-C₆-alkoxy; R^(b) isselected from the group consisting of halogen, OH, CN, amino, NO₂,C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₆-alkoxy,C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy, (C₁-C₆-alkoxy)-C₁-C₆-alkyl,(C₁-C₆-alkoxy)-C₁-C₆-alkoxy, (C₁-C₆-alkoxy)-C₂-C₆-alkenyl,(C₁-C₆-alkoxy)-C₂-C₆-alkynyl, C₁-C₆-alkylthio, (C₁-C₆-alkyl)sulfinyl,(C₁-C₆-alkyl)sulfonyl, (C₁-C₆-alkyl)amino, di(C₁-C₆-alkyl)amino,(C₁-C₆-alkyl)-carbonyl, (C₁-C₆-alkoxy)-carbonyl,(C₁-C₆-alkyl)-carbonyloxy, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkoxy,(C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy,(C₃-C₆-cycloalkoxy)-C₁-C₄-alkyl, (C₃-C₆-cycloalkyl)-carbonyloxy, wherethe aliphatic and cycloaliphatic parts of the 24 aforementioned radicalsare unsubstituted, partly or completely halogenated and where thecycloaliphatic parts of the last 6 mentioned radicals may carry 1, 2, 3,4, 5 or 6 methyl groups, for q=2 or 3 it being possible that R^(b) areidentical or different; R¹ is selected from the group consisting of H,OH, S(O)₂NH₂, CN, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,(C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₁-C₆-alkoxy,(C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkyl)carbonyl,(C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl,(C₁-C₆-alkyl)sulfonyl, (C₁-C₆-alkylamino)carbonyl,di(C₁-C₆-alkyl)aminocarbonyl, (C₁-C₆-alkylamino)sulfonyl,di(C₁-C₆-alkyl)aminosulfonyl and (C₁-C₆-alkoxy)sulfonyl, where thealiphatic and cycloaliphatic parts of the 15 aforementioned radicals areunsubstituted, partly or completely halogenated, phenyl,phenyl-C₁-C₆-alkyl, phenylsulfonyl, phenylaminosulfonyl, phenylcarbonyland phenoxycarbonyl, wherein phenyl in the last 6 mentioned radicals areunsubstituted or substituted by 1, 2, 3, 4 or 5 identical or differentsubstituents selected from the group consisting of halogen, CN, NO₂,C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy and C₁-C₆-haloalkoxy; R² isselected from the group consisting of H, OH, S(O)₂NH₂, CN, C₁-C₆-alkyl,C₂-C₆-alkenyl, C₂-C₆-alkynyl, (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl,C₁-C₆-alkoxy, (C₁-C₆-alkoxy)-C₁-C₆-alkyl, (C₁-C₆-alkyl)carbonyl,(C₃-C₆-cycloalkyl)carbonyl, (C₁-C₆-alkoxy)carbonyl,(C₁-C₆-alkyl)sulfonyl, (C₁-C₆-alkylamino)carbonyl,di(C₁-C₆-alkyl)aminocarbonyl, (C₁-C₆-alkylamino)sulfonyl,di(C₁-C₆-alkyl)aminosulfonyl and (C₁-C₆-alkoxy)sulfonyl, where thealiphatic and cycloaliphatic parts of the 15 aforementioned radicals areunsubstituted, partly or completely halogenated, phenyl, phenylsulfonyl,phenylaminosulfonyl, phenyl-C₁-C₆ alkyl, phenoxy, phenylcarbonyl andphenoxycarbonyl, wherein phenyl in the last 6 mentioned radicals isunsubstituted or substituted by 1, 2, 3, 4 or 5 identical or differentsubstituents selected from the group consisting of halogen, CN, NO₂,C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy and C₁-C₆-haloalkoxy; R³ isselected from the group consisting of H, halogen, OH, CN, C₁-C₆-alkyl,(C₁-C₆-alkoxy)-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,(C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyloxy,C₂-C₆-alkynyloxy, C₃-C₆-cycloalkoxy, (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy,where the aliphatic and cycloaliphatic parts of the 9 aforementionedradicals are unsubstituted, partly or completely halogenated; R⁴ isselected from the group consisting of H, halogen, CN, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, C₁-C₆-alkoxyand C₁-C₆-haloalkoxy; R⁵ is selected from the group consisting ofhalogen, CN, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₃-C₆-alkynyl,C₃-C₆-cycloalkyl, (C₃-C₆-cycloalkyl)-C₁-C₄-alkyl, C₃-C₆-cycloalkenyl andC₁-C₆-alkoxy-C₁-C₆-alkyl, where the aliphatic and cycloaliphatic partsof the 7 aforementioned radicals are unsubstituted, partly or completelyhalogenated; or R⁴ and R⁵ together with the carbon atom to which theyare attached may form a moiety selected from the group consisting ofcarbonyl, C₃-C₆-cycloalkan-1,1-diyl, ipso-C₃-C₆-cycloalkendiyl, three-to six-membered saturated or partially unsaturated ipso-heterocyclodiyl,where the carbocycle and the heterocycle are unsubstituted, partly orcompletely halogenated or carry from 1 to 6 C₁-C₆-alkyl groups, and themoiety >C═CR^(x)R^(y), where R^(x) and R^(y) are hydrogen, C₁-C₄-alkylor C₁-C₄-haloalkyl; including their agriculturally acceptable salts. 19.The compound of claim 18, wherein R^(a) is selected from the groupconsisting of C₁-C₆-haloalkoxy, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy,C₂-C₆-alkynyloxy, C₂-C₆-haloalkynyloxy, (C₁-C₆-alkoxy)-C₁-C₆-alkoxy,C₃-C₆-cycloalkoxy, C₃-C₆-halocycloalkoxy,(C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy and (C₃-C₆-halocycloalkyl)-C₁-C₄-alkoxy.20. The compound of claim 18, wherein R^(a) is C₃-C₆-cycloalkoxy,C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy or (C₃-C₆-cycloalkyl)-C₁-C₄-alkoxy.21. The compound of claim 18, wherein R^(b) is selected from the groupconsisting of halogen, CN, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,C₃-C₆-cycloalkoxy and C₃-C₆-halocycloalkoxy.
 22. The compound of claim18, wherein the moiety

is represented by the moiety R

wherein R^(a) is as defined in claim 18 and wherein R^(b1), R^(b2) andR^(b3) are identical or different and are hydrogen or have one of themeanings of R^(b) defined in claim
 18. 23. The compound of claim 21,wherein R^(b1), R^(b2) and R^(b3) are selected from the group consistingof and hydrogen and fluorine.
 24. The compound of claim 18, wherein themoiety

is selected from the group consisting of2-fluoro-6-(cyclopropyloxy)phenyl, 2-fluoro-6-(cyclobutyloxy)phenyl,2-fluoro-6-(cyclopentyloxy)phenyl, 2-fluoro-6-(cyclohexyloxy)phenyl,2-fluoro-6-[(cyclopropyl)methyloxy]phenyl,2-fluoro-6-[(cyclobutyl)methyloxy]phenyl,2-fluoro-6-[(cyclopentyl)methyloxy]phenyl,2-fluoro-6-[(cyclohexyl)methyloxy]phenyl, 2-fluoro-6-prop-2-enoxyphenyl,2-fluoro-6-prop-2-ynoxyphenyl, 2,3-difluoro-6-(cyclopropyloxy)phenyl,2,3-difluoro-6-(cyclobutyloxy)phenyl,2,3-difluoro-6-(cyclopentyloxy)phenyl,2,3-difluoro-6-(cyclohexyloxy)phenyl,2,3-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3-difluoro-6-prop-2-enoxyphenyl, 2,3-difluoro-6-prop-2-ynoxyphenyl,2,4-difluoro-6-(cyclopropyloxy)phenyl,2,4-difluoro-6-(cyclobutyloxy)phenyl,2,4-difluoro-6-(cyclopentyloxy)phenyl,2,4-difluoro-6-(cyclohexyloxy)phenyl,2,4-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,4-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,4-difluoro-6-prop-2-enoxyphenyl, 2,4-difluoro-6-prop-2-ynoxyphenyl,2,5-difluoro-6-(cyclopropyloxy)phenyl,2,5-difluoro-6-(cyclobutyloxy)phenyl,2,5-difluoro-6-(cyclopentyloxy)phenyl,2,5-difluoro-6-(cyclohexyloxy)phenyl,2,5-difluoro-6-[(cyclopropyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclobutyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclopentyl)methyloxy]phenyl,2,5-difluoro-6-[(cyclohexyl)methyloxy]phenyl,2,5-difluoro-6-prop-2-enoxyphenyl, 2,5-difluoro-6-prop-2-ynoxyphenyl,2,3,5-trifluoro-6-(cyclopropyloxy)phenyl,2,3,5-tifluoro-6-(cyclobutyloxy)phenyl,2,3,5-trifluoro-6-(cyclopentyloxy)phenyl,2,3,5-tifluoro-6-(cyclohexyloxy)phenyl,2,3,5-tifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,5-trifluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3,5-tifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,5-tifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,5-trifluoro-6-prop-2-enoxyphenyl,2,3,5-tifluoro-6-prop-2-ynoxyphenyl,2,4,5-trifluoro-6-(cyclopropyloxy)phenyl,2,4,5-tifluoro-6-(cyclobutyloxy)phenyl,2,4,5-trifluoro-6-(cyclopentyloxy)phenyl,2,4,5-tifluoro-6-(cyclohexyloxy)phenyl,2,4,5-tifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,4,5-trifluoro-6-[(cyclobutyl)methyloxy]phenyl,2,4,5-tifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,4,5-tifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,4,5-trifluoro-6-prop-2-enoxyphenyl,2,4,5-tifluoro-6-prop-2-ynoxyphenyl,2,3,4-trifluoro-6-(cyclopropyloxy)phenyl,2,3,4-tifluoro-6-(cyclobutyloxy)phenyl,2,3,4-trifluoro-6-(cyclopentyloxy)phenyl,2,3,4-tifluoro-6-(cyclohexyloxy)phenyl,2,3,4-tifluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3,4-tifluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,4-trifluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,4-trifluoro-6-prop-2-enoxyphenyl,2,3,4-trifluoro-6-prop-2-ynoxyphenyl,2,3,4,5-tetrafluoro-6-(cyclopropyloxy)phenyl,2,3,4,5-tetrafluoro-6-(cyclobutyl-oxy)phenyl,2,3,4,5-tetrafluoro-6-(cyclopentyloxy)phenyl,2,3,4,5-tetrafluoro-6-(cyclohexyloxy)phenyl,2,3,4,5-tetrafluoro-6-[(cyclopropyl)methyloxy]phenyl,2,3,4,5-tetrafluoro-6-[(cyclobutyl)methyloxy]phenyl,2,3,4,5-tetrafluoro-6-[(cyclopentyl)methyloxy]phenyl,2,3,4,5-tetrafluoro-6-[(cyclohexyl)methyloxy]phenyl,2,3,4,5-tetrafluoro-6-prop-2-enoxyphenyl and2,3,4,5-tetrafluoro-6-prop-2-ynoxyphenyl.
 25. The compound of claim 18,wherein R¹ is H, CN, C₁-C₄-alkyl, (C₁-C₄-alkoxy)-C₁-C₄-alkyl,C₁-C₄-alkoxy, (C₁-C₄-alkyl)carbonyl, (C₃-C₅-cycloalkyl)carbonyl or(C₁-C₄-alkyl)sulfonyl.
 26. The compound of claim 25, wherein R¹ is H.27. The compound of claim 18, wherein R² is H, CN, C₁-C₄-alkyl,(C₁-C₄-alkoxy)-C₁-C₄-alkyl, (C₁-C₄-alkyl)carbonyl,(C₃-C₅-cycloalkyl)carbonyl or (C₁-C₄-alkyl)sulfonyl.
 28. The compound ofclaim 27, wherein R² is H.
 29. The compound of claim 18, wherein R³ isselected from the group consisting of hydrogen, fluorine, chlorine,C₁-C₄-alkyl and C₁-C₄-alkoxy.
 30. The compound of claim 18, wherein R⁴is selected from the group consisting of hydrogen, fluorine,C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy and C₁-C₆-haloalkoxy.
 31. Thecompound of claim 18, wherein R⁵ is selected from the group consistingof C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₃-C₆-alkynyl,C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl, and C₁-C₆-alkoxy-C₁-C₆-alkyl. 32.The compound of claim 18, wherein R⁴ and R⁵ together with the carbonatom to which they are attached form a moiety selected from the groupconsisting of C₃-C₆-cycloalkan-1,1-diyl, ipso-C₃-C₆-cycloalkendiyl andthree- to six-membered saturated or partially unsaturatedipso-heterocyclodiyl.
 33. The compound of claim 18, wherein thecombination of R³, R⁴ and R⁵ are as given in the lines 1 to 64 of thefollowing table: # R³ R⁴ R⁵ 1 H CH₃ CH₃ 2 F F CH₃ 3 F H CH₃ 4 F CH₃ CH₃5 CH₃ CH₃ CH₃ 6 F H C₂H₅ 7 H CH₃ C₂H₅ 8 F CH₃ C₂H₅ 9 H OCH₃ CH₃ 10 HOCH₃ C₂H₅ 11 F C₂H₅ C₂H₅ 12 H OCH₃ C₂H₅ 13 H H CH(CH₃)₂ 14 H F CH(CH₃)₂15 F F CH(CH₃)₂ 16 H CH₃ CH(CH₃)₂ 17 H OCH₃ CH(CH₃)₂ 18 F CH₃ CH(CH₃)₂19 H H CH₂CH₂CH₃ 20 H F CH₂CH₂CH₃ 21 F F CH₂CH₂CH₃ 22 H CH₃ CH₂CH₂CH₃ 23H OCH₃ CH₂CH₂CH₃ 24 F CH₃ CH₂CH₂CH₃ 25 H H C(CH₃)₃ 26 H F C(CH₃)₃ 27 F FC(CH₃)₃ 28 H CH₃ C(CH₃)₃ 29 H OCH₃ C(CH₃)₃ 30 F CH₃ C(CH₃)₃ 31 H HCyclopropyl 32 H F Cyclopropyl 33 F F Cyclopropyl 34 H CH₃ Cyclopropyl35 H OCH₃ Cyclopropyl 36 F CH₃ Cyclopropyl 37 H CH₃ CF₃ 38 F CH₃ CF₃ 39H CH₂—CH₂ 40 CH₃ CH₂—CH₂ 41 OCH₃ CH₂—CH₂ 42 F CH₂—CH₂ 43 Cl CH₂—CH₂ 44 HCH₂—CH₂—CH₂ 45 CH₃ CH₂—CH₂—CH₂ 46 OCH₃ CH₂—CH₂—CH₂ 47 F CH₂—CH₂—CH₂ 48Cl CH₂—CH₂—CH₂ 49 H CH₂—CH₂—CH₂—CH₂ 50 CH₃ CH₂—CH₂—CH₂—CH₂ 51 OCH₃CH₂—CH₂—CH₂—CH₂ 52 F CH₂—CH₂—CH₂—CH₂ 53 Cl CH₂—CH₂—CH₂—CH₂ 54 HCH₂—CH₂—CH₂—CH₂—CH₂ 55 CH₃ CH₂—CH₂—CH₂—CH₂—CH₂ 56 OCH₃CH₂—CH₂—CH₂—CH₂—CH₂ 57 F CH₂—CH₂—CH₂—CH₂—CH₂ 58 Cl CH₂—CH₂—CH₂—CH₂—CH₂59 H O—CH₂—CH₂—CH₂ 60 CH₃ O—CH₂—CH₂—CH₂ 61 OCF₃ O—CH₂—CH₂—CH₂ 62 HO—CH₂—CH₂—CH₂—CH₂ 63 CH₃ O—CH₂—CH₂—CH₂—CH₂ 64 OCF₃ O—CH₂—CH₂—CH₂—CH₂


34. An agrochemical composition comprising a herbicidal active amount ofat least one compound as claimed in claim 18 and at least one inertliquid and/or solid carrier and, if appropriate, at least onesurface-active substances.
 35. A method of controlling undesiredvegetation, which comprises allowing a herbicidally active amount of atleast one compound as claimed in claim 18 to act on plants, theirenvironment or on seed.
 36. A method for the desiccation/defoliation ofplants comprising allowing a composition comprising a compound of claim18 to act on plants, their environment or on seed.